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Genome Research|November 8, 2019
Clonal copy-number mosaicism in autoreactive T lymphocytes in diabetic NOD miceMaha Alriyami, Luc Marchand, Quan Li, et al.
The Journal of Clinical Endocrinology and Metabolism|November 9, 2004
The insulin-like growth factor-II receptor gene is associated with type 1 diabetes: evidence of a maternal effectJennifer A McCann, Yong Qin Xu, Rosalie Frechette, et al.
BMC Genomics|August 19, 2006
Strand bias in complementary single-nucleotide polymorphisms of transcribed human sequences: evidence for functional effects of synonymous polymorphismsHui-Qi Qu, Steve G Lawrence, Fan Guo, et al.
Health Education Research|July 21, 2009
Compensatory beliefs about glucose testing are associated with low adherence to treatment and poor metabolic control in adolescents with type 1 diabetesMarjorie A Rabiau, Bärbel Knäuper, Thien-Kim Nguyen, et al.
Pediatric Endocrinology Reviews : PER|October 23, 2008
Mauriac syndrome: growth failure and type 1 diabetes mellitusMimi S Kim, J B Quintos
Seminars in Reproductive Medicine|June 17, 2009
Cardiovascular disease risk in adult women with congenital adrenal hyperplasia due to 21-hydroxylase deficiencyMimi S Kim, Deborah P Merke
Molecular Immunology|November 30, 2006
No association of type 1 diabetes with a functional polymorphism of the LRAP geneHui-Qi Qu, Luc Marchand, Rosalie Fréchette, et al.
Diabetes/Metabolism Research and Reviews|August 7, 2012
Overexpression of ZAC impairs glucose-stimulated insulin translation and secretion in clonal pancreatic beta-cellsXiaoyu Du, Houria Ounissi-Benkalha, Merewyn K Loder, et al.
Human Genetics|July 4, 2013
Where genotype is not predictive of phenotype: towards an understanding of the molecular basis of reduced penetrance in human inherited diseaseDavid N Cooper, Michael Krawczak, Constantin Polychronakos, et al.
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|January 21, 2015
A founder AGL mutation causing glycogen storage disease type IIIa in Inuit identified through whole-exome sequencing: a case seriesIsabelle Rousseau-Nepton, Minoru Okubo, Rosemarie Grabs, et al.
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