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http://scihub22266oqcxt.onion/ 7847376/?report=reader!1801118!7847376     free     free     free Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 243.2 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 243.2 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 243.2 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Am+J+Hum+Genet 1995 ; 56 (2): 416-21 Nephropedia Template TP {{tp|p=7847376|t=1995. Homozygosity mapping, to chromosome 11p, of the gene for familial persistent hyperinsulinemic hypoglycemia of infancy |pdf=|usr=}}{{7847376}} gab.com Text Homozygosity mapping, to chromosome 11p, of the gene for familial persistent hyperinsulinemic hypoglycemia of infancy JO: Am J Hum Genet http://www.kidney.de/pget.php?&tw=1&pmid=7847376 #FOAvip Familial persistent hyperinsulinemic hypoglycemia of infancy (PHHI) is a rare, autosomal recessive disease of unregulated insulin secretion, defined by elevations in serum insulin despite severe hypoglycemia. We used the homozygosity gene-mapping strategy to localize this disorder to the region of chromosome 11p between markers D11S1334 and D11S899 (maximum LOD score 5.02 [theta = 0] at marker D11S926) in five consanguineous families of Saudi Arabian origin. These results extend those of a recent report that also placed PHHI on chromosome 11p, between markers D11S926 and D11S928. Comparison of the boundaries of these two overlapping regions allows the PHHI locus to be assigned to the 4-cM region between the markers D11S926 and D11S899. Identification of this gene may allow a better understanding of other disorders of glucose homeostasis, by providing insight into the regulation of insulin release. Twit Text FOAVip Homozygosity mapping, to chromosome 11p, of the gene for familial persistent hyperinsulinemic hypoglycemia of infancy ????Am J Hum Genet http://www.kidney.de/pget.php?&tw=1&pmid=7847376 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=7847376 #FOAvip English Wikipedia <ref>{{Cite pmid|7847376}}</ref> Homozygosity mapping, to chromosome 11p, of the gene for familial persistent hyperinsulinemic hypoglycemia of infancy #MMPMID7847376 Thomas PM; Cote GJ; Hallman DM; Mathew PM Am J Hum Genet 1995[Feb]; 56 (2): 416-21 PMID7847376show ga Familial persistent hyperinsulinemic hypoglycemia of infancy (PHHI) is a rare, autosomal recessive disease of unregulated insulin secretion, defined by elevations in serum insulin despite severe hypoglycemia. We used the homozygosity gene-mapping strategy to localize this disorder to the region of chromosome 11p between markers D11S1334 and D11S899 (maximum LOD score 5.02 [theta = 0] at marker D11S926) in five consanguineous families of Saudi Arabian origin. These results extend those of a recent report that also placed PHHI on chromosome 11p, between markers D11S926 and D11S928. Comparison of the boundaries of these two overlapping regions allows the PHHI locus to be assigned to the 4-cM region between the markers D11S926 and D11S899. Identification of this gene may allow a better understanding of other disorders of glucose homeostasis, by providing insight into the regulation of insulin release. |*Chromosomes, Human, Pair 11[MESH] |Chromosome Mapping[MESH] |Female[MESH] |Genes, Recessive[MESH] |Genetic Linkage[MESH] |Genetic Markers[MESH] |Haplotypes[MESH] |Homozygote[MESH] |Humans[MESH] |Hyperinsulinism/physiopathology[MESH] |Hypoglycemia/physiopathology[MESH] |Infant, Newborn[MESH] |Insulin Secretion[MESH] |Insulin/metabolism[MESH] |Islets of Langerhans/embryology[MESH] |Lod Score[MESH] |Male[MESH] |Pancreatic Diseases/congenital/*genetics/physiopathology[MESH]Homozygosity mapping, to chromosome 11p, of the gene for familial pers(epmc).pdf DeepDyve Pubget Overpricing