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P S Thornton

Showing results (21-30 of 28) with videos related to

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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.
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.
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.
The New England Journal of Medicine|January 22, 1998
Familial hyperinsulinism caused by an activating glucokinase mutationB Glaser, P Kesavan, M Heyman, 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.
Diabetes|March 29, 2001
Dysregulation of insulin secretion in children with congenital hyperinsulinism due to sulfonylurea receptor mutationsA Grimberg, R J Ferry, A Kelly, 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.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|August 8, 2016
Cutaneous skeletal hypophosphatemia syndrome: clinical spectrum, natural history, and treatmentD Ovejero, Y H Lim, A M Boyce, et al.
Pageof 3

Showing results (21-30 of 28) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 28 results.
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.
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.
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.
The New England Journal of Medicine|January 22, 1998
Familial hyperinsulinism caused by an activating glucokinase mutationB Glaser, P Kesavan, M Heyman, 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.
Diabetes|March 29, 2001
Dysregulation of insulin secretion in children with congenital hyperinsulinism due to sulfonylurea receptor mutationsA Grimberg, R J Ferry, A Kelly, 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.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|August 8, 2016
Cutaneous skeletal hypophosphatemia syndrome: clinical spectrum, natural history, and treatmentD Ovejero, Y H Lim, A M Boyce, et al.
Pageof 3