Human genetics (BASKET)

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Human genetics (BASKET)

LE WE PMID CA

Human genetics (BASKET)

1232

Humangenetik (allg)

Bayesian statistics

Data base (Medicine Biology Pharmacology)

Eye and orbita (Inherited diseases)

Human genetics (BASKET)

Medical ethics

Neoplasia (Tumor biology and immunology)

RNA (MicroRNA)

1989 1	ABC of clinical genetics. DNA analysis in genetic disorders. [2527577] BMJ 299(6692): 170-4 (1989)
1989 2	ABC of clinical genetics. Techniques of DNA analysis. [2569341] BMJ 299(6690): 34-7 (1989)
1989 3	ABC of clinical genetics. Gene structure and function. [2503156] BMJ 298(6688): 1629-31 (1989)
1989 4	ABC of clinical genetics. Chromosomal disorders II. [2523747] BMJ 298(6676): 813-6 (1989)
1989 5	ABC of clinical genetics. Mendelian inheritance. [2493942] BMJ 298(6670): 375-8 (1989)
2009 6	Genetics and the general physician: insights, applications and future challenges. [19737788] QJM 102(11): 757-72 (2009)
1997 7	Adult-onset genetic disease: mechanisms, analysis and prediction. [9068799] QJM 90(2): 83-103 (1997)
2003 8	The challenges of recording phenotype in a generalizable and computable form. [12629577] Pharmacogenomics J 3(1): 8-10 (2003)
2008 9	What is ideal genetic counselling? A survey of current international guidelines. [18197196] Eur J Hum Genet 16(4): 445-52 (2008)
1986 10	DNA analysis in human disease. [3543064] J Clin Pathol 39(12): 1281-95 (1986)
1991 11	Medical genetics. [1924046] Postgrad Med J 67(789): 613-31 (1991)
1979 12	Ascites production in 9 rat strains. [312305] J Immunol Methods 26(1): 69-74 (1979)
2002 13	Medical genetics: 2. The diagnostic approach to the child with dysmorphic signs. [12197694] CMAJ 167(4): 367-72 (2002)
2002 14	Medical genetics: 1. Clinical teratology in the age of genomics. [12186175] CMAJ 167(3): 265-73 (2002)
2010 15	From the laboratory to the clinic: molecular genetic testing in pediatric ophthalmology. [20103038] Am J Ophthalmol 149(1): 10-17 (2010)
2010 16	Fine-scale population structure and the era of next-generation sequencing. [20876616] Hum Mol Genet 19(R2): R221-6 (2010)
2010 17	Evolutionary history of regulatory variation in human populations. [20876617] Hum Mol Genet 19(R2): R197-203 (2010)
2010 18	Loss-of-function variants in the genomes of healthy humans. [20805107] Hum Mol Genet 19(R2): R125-30 (2010)
2010 19	Phenotypic variability and genetic susceptibility to genomic disorders. [20807775] Hum Mol Genet 19(R2): R176-87 (2010)
2009 20	Lessons learnt from large-scale exon re-sequencing of the X chromosome. [19297402] Hum Mol Genet 18(R1): R60-4 (2009)
2009 21	The resolution of the genetics of gene expression. [19808798] Hum Mol Genet 18(R2): R211-5 (2009)
2010 22	Clinical and public health implications of emerging genetic technologies. [20347647] Semin Nephrol 30(2): 185-94 (2010)
2007 23	Dysmorphology demystified. [17449858] Arch Dis Child Fetal Neonatal Ed 92(3): F225-9 (2007)
2009 24	Genetic testing in asymptomatic minors: Recommendations of the European Society of Human Genetics. [19277059] Eur J Hum Genet 17(6): 720-1 (2009)
2009 25	Genetic testing in asymptomatic minors: background considerations towards ESHG Recommendations. [19277061] Eur J Hum Genet 17(6): 711-9 (2009)
2008 26	Rapid aneuploidy testing versus traditional karyotyping: is it better to know more? [18239236] Hong Kong Med J 14(1): 4-5 (2008)
2006 27	Genetic diagnosis and testing in clinical practice. [16809405] Clin Med Res 4(2): 123-9 (2006)
2011 28	Single-nucleotide polymorphisms among microRNA: big effects on cancer. [21627860] Chin J Cancer 30(6): 381-91 (2011)
2011 29	Genetic diagnostic methods for inherited eye diseases. [21572730] Middle East Afr J Ophthalmol 18(1): 24-9 (2011)
2010 30	Ethical issues raised by common copy number variants and single nucleotide polymorphisms of certain and uncertain significance in general medical practice. [20642868] Genome Med 2(7): 42 (2010)
2009 31	The Human Gene Mutation Database: providing a comprehensive central mutation database for molecular diagnostics and personalized genomics. [20038494] Hum Genomics 4(2): 69-72 (2009)
2004 32	Bayesian analysis and risk assessment in genetic counseling and testing. [14736820] J Mol Diagn 6(1): 1-9 (2004)
2009 33	PrognoScan: a new database for meta-analysis of the prognostic value of genes. [19393097] BMC Med Genomics 2(-): 18 (2009)
2010 34	Beyond genome-wide association studies: genetic heterogeneity and individual predisposition to cancer. [20106545] Trends Genet 26(3): 132-41 (2010)
2010 35	Array-based technology and recommendations for utilization in medical genetics practice for detection of chromosomal abnormalities. [20962661] Genet Med 12(11): 742-5 (2010)
PMC 36	Return of genetic results in the familial dilated cardiomyopathy research project. [22886719] J Genet Couns 22(2):164-74 (2013)

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