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The Journal of Pediatrics|February 21, 1998
Familial hyperinsulinism with apparent autosomal dominant inheritance: clinical and genetic differences from the autosomal recessive variantP S Thornton, M S Satin-Smith, K Herold, et al.Science (New York, N.Y.)|June 21, 1996
Adenosine diphosphate as an intracellular regulator of insulin secretionC G Nichols, S L Shyng, A Nestorowicz, et al.Nature Genetics|June 1, 1994
Familial hyperinsulinism maps to chromosome 11p14-15.1, 30 cM centromeric to the insulin geneB Glaser, K C Chiu, R Anker, et al.Human Molecular Genetics|May 1, 1995
Recombinant mapping of the familial hyperinsulinism gene to an 0.8 cM region on chromosome 11p15.1 and demonstration of a founder effect in Ashkenazi JewsB Glaser, K C Chiu, L Liu, et al.Diabetes|November 14, 1997
A nonsense mutation in the inward rectifier potassium channel gene, Kir6.2, is associated with familial hyperinsulinismA Nestorowicz, N Inagaki, T Gonoi, et al.Human Molecular Genetics|November 1, 1996
Mutations in the sulonylurea receptor gene are associated with familial hyperinsulinism in Ashkenazi JewsA Nestorowicz, B A Wilson, K P Schoor, et al.Pageof 4