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Educational Case: Wilms Tumor (Nephroblastoma).

Acad Pathol 2019; 6 ():

*30733996*
                       30733996

Educational Case: Wilms Tumor.

Acad Pathol 2018; 5 ():

*30140735*
                       30140735

Mesenchymal Hamartoma of the Liver in an Infant With Beckwith-Wiedemann Syndrome: A Rare Condition Mimicking Hepatoblastoma.

ACG Case Rep J 2015; 2 (4): 258-60

*26203458*
                       26203458

JAK2 V617F MUTATION SCANNING IN PATIENTS WITH ADRENAL INCIDENTALOMA.

Acta Endocrinol (Buchar) 2017; 13 (2): 150-3

*31149166*
                       31149166

Gray matter injury associated with periventricular leukomalacia in the premature infant.

Acta Neuropathol 2007; 114 (6): 619-31

*17912538*
                       17912538

Comparative untargeted proteomic analysis of ADME proteins and tumor antigens for tumor cell lines.

Acta Pharm Sin B 2018; 8 (2): 252-60

*29719786*
                       29719786

Stem cells and small molecule screening: haploid embryonic stem cells as a new tool.

Acta Pharmacol Sin 2013; 34 (6): 725-31

*23645011*
                       23645011

Perturbations to the IGF1 growth pathway and adult energy homeostasis following disruption of mouse chromosome 12 imprinting.

Acta Physiol (Oxf) 2014; 210 (1): 174-87

*24034272*
                       24034272

Breast fibroadenomas in adolescents: current perspectives.

Adolesc Health Med Ther 2015; 6 (): 159-63

*26366109*
                       26366109

Rhabdomyosarcoma in adolescent and young adult patients: current perspectives.

Adolesc Health Med Ther 2014; 5 (): 115-25

*24966711*
                       24966711

Chromatin Insulators: A Role in Nuclear Organization and Gene Expression.

Adv Cancer Res 2011; 110 (): 43-76

  • Genetics (Insulator)
  • *21704228*
                           21704228

    Principles and Pitfalls in the Differential Diagnosis and Management of Childhood Obesities123.

    Adv Nutr 2014; 5 (3): 299S-305S

    *24829481*
                           24829481

    Wilms Tumor.

    Adv Pediatr 2012; 59 (1): 247-67

    *22789581*
                           22789581

    Wilms? tumour: Determinants of prognosis in an African setting.

    Afr J Paediatr Surg 2015; 12 (3): 171-6

    *26612121*
                           26612121

    The negative effect of prolonged somatotrophic/insulin signaling on an adult bone marrow-residing population of pluripotent very small embryonic-like stem cells (VSELs).

    Age (Dordr) 2013; 35 (2): 315-30

    *22218782*
                           22218782

    Relationship of p21WAF1/CIP1/SDI1 to cell proliferation in primary cultures of adrenocortical cells.

    Age (Omaha) 1999; 22 (2): 39-44

    *23604395*
                           23604395

    Intrauterine Growth Restriction Associated with Hematologic Abnormalities: Probable Manifestations of Placental Mesenchymal Dysplasia.

    AJP Rep 2015; 5 (2): e085-8

    *26495159*
                           26495159

    Clitoral Epidermoid Cyst Presenting as Pseudoclitoromegaly of Pregnancy.

    AJP Rep 2013; 3 (1): 57-62

    *23943712*
                           23943712

    How Accurately Does Current Fetal Imaging Identify Posterior Fossa Anomalies?

    AJR Am J Roentgenol 2008; 190 (6): 1637-43

    *18492918*
                           18492918

    Role of the zinc finger and SCAN domain-containing transcription factors in cancer.

    Am J Cancer Res 2019; 9 (5): 816-36

    *31218096*
                           31218096

    Long non-coding RNA Linc00152 is a positive prognostic factor for and demonstrates malignant biological behavior in clear cell renal cell carcinoma.

    Am J Cancer Res 2016; 6 (2): 285-99

    *27186403*
                           27186403

    mRNA and microRNA expression patterns in adrenocortical cancer.

    Am J Cancer Res 2011; 1 (5): 618-28

    *21994902*
                           21994902

    Therapy of adrenocortical cancer: present and future.

    Am J Cancer Res 2011; 1 (2): 222-32

    *21969107*
                           21969107

    Placental Pathology in Placental Mesenchymal Dysplasia with 13q12.11 Deletion and a 25-Week Gestation Female Infant.

    Am J Case Rep 2018; 19 (): 369-73

    *29593209*
                           29593209

    Perinatal Case of Fatal Simpson-Golabi-Behmel Syndrome with Hyperplasia of Seminiferous Tubules.

    Am J Case Rep 2017; 18 (): 649-55

    *28600484*
                           28600484

    Neonatal Genome-Wide Methylation Patterns in Relation to Birth Weight in the Norwegian Mother and Child Cohort.

    Am J Epidemiol 2014; 179 (7): 834-42

    *24561991*
                           24561991

    Advanced Parental Age and the Risk of Autism Spectrum Disorder.

    Am J Epidemiol 2008; 168 (11): 1268-76

    *18945690*
                           18945690

    Growth perturbations in a phenotype with rapid fetal growth preceding preterm labor and term birth.

    Am J Hum Biol 2009; 21 (6): 782-92

    *19298010*
                           19298010

    Bi-allelic TMEM94 Truncating Variants Are Associated with Neurodevelopmental Delay, Congenital Heart Defects, and Distinct Facial Dysmorphism.

    Am J Hum Genet 2018; 103 (6): 948-67

    *30526868*
                           30526868

    Genomic DNA Methylation Signatures Enable Concurrent Diagnosis and Clinical Genetic Variant Classification in Neurodevelopmental Syndromes.

    Am J Hum Genet 2018; 102 (1): 156-74

    *29304373*
                           29304373

    Mutations in Epigenetic Regulation Genes Are a Major Cause of Overgrowth with Intellectual Disability.

    Am J Hum Genet 2017; 100 (5): 725-36

    *28475857*
                           28475857

    Detection of Imprinted Genes by Single-Cell Allele-Specific Gene Expression.

    Am J Hum Genet 2017; 100 (3): 444-53

    *28190458*
                           28190458

    Allele-Specific Methylome and Transcriptome Analysis Reveals Widespread Imprinting in the Human Placenta.

    Am J Hum Genet 2016; 99 (5): 1045-58

    *27843122*
                           27843122

    DNA Methylation Profiling of Uniparental Disomy Subjects Provides a Map of Parental Epigenetic Bias in the Human Genome.

    Am J Hum Genet 2016; 99 (3): 555-66

    *27569549*
                           27569549

    Gene-centric Meta-analysis in 87,736 Individuals of European Ancestry Identifies Multiple Blood-Pressure-Related Loci.

    Am J Hum Genet 2014; 94 (3): 349-60

    *24560520*
                           24560520

    De Novo Mutations in the Genome Organizer CTCF Cause Intellectual Disability.

    Am J Hum Genet 2013; 93 (1): 124-31

    *23746550*
                           23746550

    A Palindrome-Mediated Recurrent Translocation with 3:1 Meiotic Nondisjunction: The t(8;22)(q24.13;q11.21).

    Am J Hum Genet 2010; 87 (2): 209-18

    *20673865*
                           20673865

    Distinct Effects of Allelic NFIX Mutations on Nonsense-Mediated mRNA Decay Engender Either a Sotos-like or a Marshall-Smith Syndrome.

    Am J Hum Genet 2010; 87 (2): 189-98

    *20673863*
                           20673863

    Mapping Allele-Specific DNA Methylation: A New Tool for Maximizing Information from GWAS.

    Am J Hum Genet 2010; 86 (2): 109-12

    *20159108*
                           20159108

    Massively Parallel Sequencing: The Next Big Thing in Genetic Medicine.

    Am J Hum Genet 2009; 85 (2): 142-54

    *19679224*
                           19679224

    This Month in Genetics.

    Am J Hum Genet 2008; 83 (6): 661-2

    *C2668063*
                           C2668063

    Maternally Inherited Birk Barel Mental Retardation Dysmorphism Syndrome Caused by a Mutation in the Genomically Imprinted Potassium Channel KCNK9.

    Am J Hum Genet 2008; 83 (2): 193-9

    *18678320*
                           18678320

    Allan Award Lecture: Rare Patients Leading to Epigenetics and Back to Genetics.

    Am J Hum Genet 2008; 82 (5): 1034-8

    *18468009*
                           18468009

    Epigenomic Profiling Reveals DNA-Methylation Changes Associated with Major Psychosis.

    Am J Hum Genet 2008; 82 (3): 696-711

    *18319075*
                           18319075

    Genetic Factors in Congenital Diaphragmatic Hernia.

    Am J Hum Genet 2007; 80 (5): 825-45

  • Diaphragmatic hernia (congenital)
  • *17436238*
                           17436238

    Mendelian Inheritance in Man and Its Online Version, OMIM.

    Am J Hum Genet 2007; 80 (4): 588-604

    *17357067*
                           17357067

    Epigenetic Allele Silencing Unveils Recessive RYR1 Mutations in Core Myopathies.

    Am J Hum Genet 2006; 79 (5): 859-68

    *17033962*
                           17033962

    Intra- and Interindividual Epigenetic Variation in Human Germ Cells.

    Am J Hum Genet 2006; 79 (1): 67-84

    *16773567*
                           16773567

    This Month in the Journal.

    Am J Hum Genet 2006; 78 (5): i-ii

    *C1474036*
                           C1474036

    Imprinting at the SMPD1 Locus: Implications for Acid Sphingomyelinase?Deficient Niemann-Pick Disease.

    Am J Hum Genet 2006; 78 (5): 865-70

    *16642440*
                           16642440

    Hypomethylation of the H19 Gene Causes Not Only Silver-Russell Syndrome (SRS) but Also Isolated Asymmetry or an SRS-Like Phenotype.

    Am J Hum Genet 2006; 78 (4): 604-14

    *16532391*
                           16532391

    Children with Idiopathic Hemihypertrophy and Beckwith-Wiedemann Syndrome Have Different Constitutional Epigenotypes Associated with Wilms Tumor.

    Am J Hum Genet 2005; 77 (5): 887-91

    *16252245*
                           16252245

    This Month in the Journal.

    Am J Hum Genet 2005; 77 (2): i-ii

    *C1224541*
                           C1224541

    Genotype-Phenotype Associations in Sotos Syndrome: An Analysis of 266 Individuals with NSD1 Aberrations.

    Am J Hum Genet 2005; 77 (2): 193-204

    *15942875*
                           15942875

    A Novel STX16 Deletion in Autosomal Dominant Pseudohypoparathyroidism Type Ib Redefines the Boundaries of a cis-Acting Imprinting Control Element of GNAS.

    Am J Hum Genet 2005; 76 (5): 804-14

    *15800843*
                           15800843

    This Month in the Journal.

    Am J Hum Genet 2005; 76 (3): i-ii

    *C1196408*
                           C1196408

    Possible Genomic Imprinting of Three Human Obesity?Related Genetic Loci.

    Am J Hum Genet 2005; 76 (3): 427-37

    *15647995*
                           15647995

    This Month in the Journal.

    Am J Hum Genet 2004; 75 (5): i-ii

    *C1182130*
                           C1182130

    Announcements1.

    Am J Hum Genet 2004; 75 (5): 930-1

    *C1182128*
                           C1182128

    Microdeletion of LIT1 in Familial Beckwith-Wiedemann Syndrome.

    Am J Hum Genet 2004; 75 (5): 844-9

    *15372379*
                           15372379

    Beckwith-Wiedemann Syndrome and IVF: A Case-Control Study.

    Am J Hum Genet 2004; 75 (3): 526-8

    *15284956*
                           15284956

    Paradoxical NSD1 Mutations in Beckwith-Wiedemann Syndrome and 11p15 Anomalies in Sotos Syndrome.

    Am J Hum Genet 2004; 74 (4): 715-20

    *14997421*
                           14997421

    Epigenetics and Assisted Reproductive Technology: A Call for Investigation.

    Am J Hum Genet 2004; 74 (4): 599-609

    *14991528*
                           14991528

    Genomic Imprinting and Linkage Test for Quantitative-Trait Loci in Extended Pedigrees.

    Am J Hum Genet 2003; 73 (4): 933-8

    *13680523*
                           13680523

    Loss of CpG Methylation Is Strongly Correlated with Loss of Histone H3 Lysine 9 Methylation at DMR-LIT1 in Patients with Beckwith-Wiedemann Syndrome.

    Am J Hum Genet 2003; 73 (4): 948-56

    *12949703*
                           12949703

    Discordance between Genetic and Epigenetic Defects in Pseudohypoparathyroidism Type 1b Revealed by Inconsistent Loss of Maternal Imprinting at GNAS1.

    Am J Hum Genet 2003; 73 (2): 314-22

    *12858292*
                           12858292

    In Vitro Fertilization May Increase the Risk of Beckwith-Wiedemann Syndrome Related to the Abnormal Imprinting of the KCNQ1OT Gene.

    Am J Hum Genet 2003; 72 (5): 1338-41

    *12772698*
                           12772698

    Overgrowth Syndromes.

    Am J Hum Genet 2003; 72 (3): 772-3

    *C1180254*
                           C1180254

    This Month in the Journal.

    Am J Hum Genet 2003; 72 (1): i-ii

    *C420017*
                           C420017

    NSD1 Mutations Are the Major Cause of Sotos Syndrome and Occur in Some Cases of Weaver Syndrome but Are Rare in Other Overgrowth Phenotypes.

    Am J Hum Genet 2003; 72 (1): 132-43

    *12464997*
                           12464997

    Association of In Vitro Fertilization with Beckwith-Wiedemann Syndrome and Epigenetic Alterations of LIT1 and H19.

    Am J Hum Genet 2003; 72 (1): 156-60

    *12439823*
                           12439823

    This Month in the Journal.

    Am J Hum Genet 2002; 70 (3): i-ii

    *C384964*
                           C384964

    Testing for Genetic Linkage in Families by a Variance-Components Approach in the Presence of Genomic Imprinting.

    Am J Hum Genet 2002; 70 (3): 751-7

    *11836650*
                           11836650

    Epigenetic Alterations of H19 and LIT1 Distinguish Patients with Beckwith-Wiedemann Syndrome with Cancer and Birth Defects.

    Am J Hum Genet 2002; 70 (3): 604-11

    *11813134*
                           11813134

    A Narrow Segment of Maternal Uniparental Disomy of Chromosome 7q31-qter in Silver-Russell Syndrome Delimits a Candidate Gene Region.

    Am J Hum Genet 2001; 68 (1): 247-53

    *11112662*
                           11112662

    Partial Paternal Uniparental Disomy of Chromosome 6 in an Infant with Neonatal Diabetes, Macroglossia, and Craniofacial Abnormalities.

    Am J Hum Genet 2000; 67 (6): 1586-91

    *11038325*
                           11038325

    This Month in the Journal.

    Am J Hum Genet 2000; 67 (4): i-ii

    *C1287904*
                           C1287904

    Mechanisms of Genomic Imprinting.

    Am J Hum Genet 2000; 67 (4): 777-87

  • Epigenetics
  • *10986038*
                           10986038

    Disruption of a novel imprinted zinc-finger gene, ZNF215, in Beckwith-Wiedemann syndrome.

    Am J Hum Genet 2000; 66 (5): 1473-84

    *10762538*
                           10762538

    Identification of Novel Imprinted Transcripts in the Prader-Willi Syndrome and Angelman Syndrome Deletion Region: Further Evidence for Regional Imprinting Control.

    Am J Hum Genet 2000; 66 (3): 848-58

    *10712201*
                           10712201

    This Month in the Journal.

    Am J Hum Genet 2000; 66 (3): i-ii

    *C1288181*
                           C1288181

    Relaxation of Insulin-like Growth Factor 2 Imprinting and Discordant Methylation at KvDMR1 in Two First Cousins Affected by Beckwith-Wiedemann and Klippel-Trenaunay-Weber Syndromes.

    Am J Hum Genet 2000; 66 (3): 841-7

    *10712200*
                           10712200

    Duplication of 7p11.2-p13, Including GRB10, in Silver-Russell Syndrome.

    Am J Hum Genet 2000; 66 (1): 36-46

    *10631135*
                           10631135

    Are There Low-Penetrance TP53 Alleles? Evidence from Childhood Adrenocortical Tumors.

    Am J Hum Genet 1999; 65 (4): 995-1006

    *10486318*
                           10486318

    Mapping of a new SGBS locus to chromosome Xp22 in a family with a severe form of Simpson-Golabi-Behmel syndrome.

    Am J Hum Genet 1999; 65 (3): 779-83

    *10441586*
                           10441586

    A chromosomal duplication map of malformations: regions of suspected haplo- and triplolethality--and tolerance of segmental aneuploidy--in humans.

    Am J Hum Genet 1999; 64 (6): 1702-8

    *10330358*
                           10330358

    Imprinting-mutation mechanisms in Prader-Willi syndrome.

    Am J Hum Genet 1999; 64 (2): 397-413

    *9973278*
                           9973278

    Uniparental disomies in unselected populations.

    Am J Hum Genet 1998; 63 (4): 962-6

  • Uniparental disomia
  • *9758632*
                           9758632

    Cytosine methylation and the unequal developmental potentials of the oocyte and sperm genomes.

    Am J Hum Genet 1998; 62 (6): 1269-73

    *9585619*
                           9585619

    Inherited interstitial duplications of proximal 15q: genotype-phenotype correlations.

    Am J Hum Genet 1997; 61 (6): 1342-52

    *9399882*
                           9399882

    Poster presentations.

    Am J Hum Genet 1997; 61 (Suppl): A264-324

    *C1712622*
                           C1712622

    Poster presentations.

    Am J Hum Genet 1997; 61 (Suppl): A59-A117

    *C1712616*
                           C1712616

    Published abstracts.

    Am J Hum Genet 1997; 61 (Suppl): A361-413

    *C1712614*
                           C1712614

    Maternal uniparental disomy of chromosome 1 with reduction to homozygosity of the LAMB3 locus in a patient with Herlitz junctional epidermolysis bullosa.

    Am J Hum Genet 1997; 61 (3): 611-9

    *9326326*
                           9326326

    Low frequency of p57KIP2 mutation in Beckwith-Wiedemann syndrome.

    Am J Hum Genet 1997; 61 (2): 304-9

    *9311734*
                           9311734

    Coding mutations in p57KIP2 are present in some cases of Beckwith-Wiedemann syndrome but are rare or absent in Wilms tumors.

    Am J Hum Genet 1997; 61 (2): 295-303

    *9311733*
                           9311733

    Different mechanisms and recurrence risks of imprinting defects in Angelman syndrome.

    Am J Hum Genet 1997; 61 (1): 88-93

    *9245988*
                           9245988

    Congenital anomalies and childhood cancer in Great Britain.

    Am J Hum Genet 1997; 60 (3): 474-85

    *9042906*
                           9042906

    A variant of Freeman-Sheldon syndrome maps to 11p15.5-pter.

    Am J Hum Genet 1997; 60 (2): 426-32

    *9012416*
                           9012416

    Fine mapping of an imprinted gene for familial nonchromaffin paragangliomas, on chromosome 11q23.

    Am J Hum Genet 1997; 60 (1): 121-32

    *8981955*
                           8981955

    Normal phenotype with maternal isodisomy in a female with two isochromosomes: i(2p) and i(2q).

    Am J Hum Genet 1996; 59 (5): 1114-8

    *8900241*
                           8900241

    Poster Presentations.

    Am J Hum Genet 1996; 59 (Suppl): A244-96

    *C1915519*
                           C1915519

    Poster Presentations.

    Am J Hum Genet 1996; 59 (Suppl): A61-A109

    *C1915518*
                           C1915518

    Slide Presentations.

    Am J Hum Genet 1996; 59 (Suppl): A3-A59

    *11644831*
                           11644831

    Inactivation of the first nucleotide-binding fold of the sulfonylurea receptor, and familial persistent hyperinsulinemic hypoglycemia of infancy.

    Am J Hum Genet 1996; 59 (3): 510-8

    *8751851*
                           8751851

    Complete paternal isodisomy for chromosome 8 unmasked by lipoprotein lipase deficiency.

    Am J Hum Genet 1996; 59 (2): 431-6

    *8755931*
                           8755931

    Heritability of X chromosome--inactivation phenotype in a large family.

    Am J Hum Genet 1996; 58 (6): 1111-9

    *8651287*
                           8651287

    Poster Presentations.

    Am J Hum Genet 1995; 57 (Suppl): A159-233

    *C1801576*
                           C1801576

    Slide Presentations.

    Am J Hum Genet 1995; 57 (Suppl): A3-A58

    *C1801573*
                           C1801573

    Poster Presentations.

    Am J Hum Genet 1995; 57 (Suppl): A59-A106

    *C1801572*
                           C1801572

    Segregation distortion in the offspring of Afro-American fathers with postaxial polydactyly.

    Am J Hum Genet 1995; 56 (5): 1207-11

    *7726178*
                           7726178

    Testing parental imprinting in insulin-dependent diabetes mellitus by the marker-association-segregation-chi 2 method.

    Am J Hum Genet 1995; 56 (5): 1080-7

    *7726162*
                           7726162

    Studies of X inactivation and isodisomy in twins provide further evidence that the X chromosome is not involved in Rett syndrome.

    Am J Hum Genet 1995; 56 (3): 647-53

    *7887418*
                           7887418

    Homozygosity mapping, to chromosome 11p, of the gene for familial persistent hyperinsulinemic hypoglycemia of infancy.

    Am J Hum Genet 1995; 56 (2): 416-21

    *7847376*
                           7847376

    A familial "balanced" 3;9 translocation with cryptic 8q insertion leading to deletion and duplication of 9p23 loci in siblings.

    Am J Hum Genet 1995; 56 (1): 302-9

    *7825591*
                           7825591

    Paternal isodisomy for chromosome 7 is compatible with normal growth and development in a patient with congenital chloride diarrhea.

    Am J Hum Genet 1994; 55 (4): 747-52

    *7942853*
                           7942853

    Uniparental isodisomy for paternal 7p and maternal 7q in a child with growth retardation.

    Am J Hum Genet 1994; 55 (2): 253-65

    *7913578*
                           7913578

    New insights reveal complex mechanisms involved in genomic imprinting.

    Am J Hum Genet 1994; 54 (5): 733-40

    *8178814*
                           8178814

    Uniparental disomy occurs infrequently in Wilms tumor patients.

    Am J Hum Genet 1994; 54 (2): 282-9

    *8304345*
                           8304345

    Maternal uniparental disomy 22 has no impact on the phenotype.

    Am J Hum Genet 1994; 54 (1): 21-4

    *8279466*
                           8279466

    Normal phenotype with paternal uniparental isodisomy for chromosome 21.

    Am J Hum Genet 1993; 53 (5): 1074-8

    *8213833*
                           8213833

    Detection of cryptic chromosomal abnormalities in unexplained mental retardation: a general strategy using hypervariable subtelomeric DNA polymorphisms.

    Am J Hum Genet 1993; 53 (3): 688-701

    *8352277*
                           8352277

    Poster presentations.

    Am J Hum Genet 1993; 53 (Suppl): 173-234

    *C1682329*
                           C1682329

    Imprinting of human H19: allele-specific CpG methylation, loss of the active allele in Wilms tumor, and potential for somatic allele switching.

    Am J Hum Genet 1993; 53 (1): 113-24

    *8391213*
                           8391213

    Maternal uniparental disomy for human chromosome 14, due to loss of a chromosome 14 from somatic cells with t(13;14) trisomy 14.

    Am J Hum Genet 1993; 52 (6): 1145-52

    *8503447*
                           8503447

    A radiation hybrid map of the distal short arm of human chromosome 11, containing the Beckwith-Wiedemann and associated embryonal tumor disease loci.

    Am J Hum Genet 1993; 52 (5): 915-21

    *8387721*
                           8387721

    Constitutional 1p36 deletion in a child with neuroblastoma.

    Am J Hum Genet 1993; 52 (1): 176-82

    *8434586*
                           8434586

    Genetic mapping of the human tryptophan hydroxylase gene on chromosome 11, using an intronic conformational polymorphism.

    Am J Hum Genet 1992; 51 (6): 1366-71

    *1463016*
                           1463016

    Poster presentations.

    Am J Hum Genet 1992; 51 (Suppl): A56-A119

    *C1683077*
                           C1683077

    Poster presentations.

    Am J Hum Genet 1992; 51 (Suppl): A181-232

    *C1683076*
                           C1683076

    Published abstracts.

    Am J Hum Genet 1992; 51 (Suppl): A273-334

    *C1683068*
                           C1683068

    Maternal uniparental isodisomy of chromosome 14: association with autosomal recessive rod monochromacy.

    Am J Hum Genet 1992; 50 (4): 690-9

    *1347967*
                           1347967

    Mapping of 262 DNA markers into 24 intervals on human chromosome 11.

    Am J Hum Genet 1992; 50 (1): 56-64

    *1346079*
                           1346079

    Introduction: Abstracts of poster presentations.

    Am J Hum Genet 1991; 49 (Suppl): 125-78

    *C1683322*
                           C1683322

    Three different frameshift mutations of the tyrosinase gene in type IA oculocutaneous albinism.

    Am J Hum Genet 1991; 49 (1): 199-206

    *1905879*
                           1905879

    Twinning and mitotic crossing-over: some possibilities and their implications.

    Am J Hum Genet 1991; 49 (1): 120-30

    *2063864*
                           2063864

    Localization of DNA sequences to a region within Xp11.21 between incontinentia pigmenti (IP1) X-chromosomal translocation breakpoints.

    Am J Hum Genet 1991; 48 (1): 53-64

    *1985463*
                           1985463

    Cancer genetics.

    Am J Hum Genet 1990; 47 (Suppl): A3-A45

    *C1683946*
                           C1683946

    Clinical genetics.

    Am J Hum Genet 1990; 47 (Suppl): A45-A106

    *C1683942*
                           C1683942

    Genomic imprinting and the Beckwith-Wiedemann syndrome.

    Am J Hum Genet 1990; 46 (5): 1000-1

    *2339685*
                           2339685

    Advances in human genetics.

    Am J Hum Genet 1990; 46 (5): 1007-8

    *C1683588*
                           C1683588

    Genomic imprinting: review and relevance to human diseases.

    Am J Hum Genet 1990; 46 (5): 857-73

    *2187341*
                           2187341

    Localization of HeLa cell tumor-suppressor gene to the long arm of chromosome II.

    Am J Hum Genet 1989; 45 (4): 565-77

    *2577469*
                           2577469

    Molecular genetics.

    Am J Hum Genet 1989; 45 (Suppl): A169-232

    *C1683451*
                           C1683451

    Clinical genetics.

    Am J Hum Genet 1989; 45 (Suppl): A38-97

    *C1683449*
                           C1683449

    Genetic linkage of Beckwith-Wiedemann syndrome to 11p15.

    Am J Hum Genet 1989; 44 (5): 720-3

    *2565083*
                           2565083

    Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5.

    Am J Hum Genet 1989; 44 (5): 711-9

    *2539717*
                           2539717

    Molecular cytogenetics: toward dissection of the contiguous gene syndromes.

    Am J Hum Genet 1988; 43 (5): 575-8

    *3189328*
                           3189328

    Clinical genetics.

    Am J Hum Genet 1988; 43 (Suppl): A36-A100

    *C1715419*
                           C1715419

    Normal dosage of the insulin and insulin-like growth factor II genes in patients with the Beckwith-Wiedemann syndrome.

    Am J Hum Genet 1986; 39 (2): 265-73

    *3529947*
                           3529947

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