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Human Heredity|January 1, 1984
Estimating the recombination frequency for the MN and the Ss lociM A Spence, L L Field, M L Marazita, et al.
The Journal of Clinical Endocrinology and Metabolism|October 16, 2001
Autoantibodies and human leucocyte antigen class II in first-degree family members of Mexican-American type 1 diabetic patientsA Zeidler, L J Raffel, G Costin, et al.
American Journal of Human Genetics|July 31, 1998
Families with familial combined hyperlipidemia and families enriched for coronary artery disease share genetic determinants for the atherogenic lipoprotein phenotypeH Allayee, B E Aouizerat, R M Cantor, et al.
Diabetes|July 1, 1992
Genetic marker associations with proliferative retinopathy in persons diagnosed with diabetes before 30 yr of ageK J Cruickshanks, C M Vadheim, S E Moss, et al.
Molecular Genetics and Metabolism|December 16, 1998
Amyloidosis in familial mediterranean fever is associated with a specific ancestral haplotype in the MEFV locusM Shohat, R Lotan, N Magal, et al.
Human Reproduction (Oxford, England)|November 30, 2018
Bidirectional Mendelian randomization to explore the causal relationships between body mass index and polycystic ovary syndromeM A Brower, Y Hai, M R Jones, et al.
American Journal of Medical Genetics|June 22, 1999
Severe achondroplasia with developmental delay and acanthosis nigricans (SADDAN): phenotypic analysis of a new skeletal dysplasia caused by a Lys650Met mutation in fibroblast growth factor receptor 3G A Bellus, M J Bamshad, K A Przylepa, et al.
Gastroenterology|February 1, 1978
Cimetidine versus intensive antacid therapy for duodenal ulcer: a multicenter trialA F Ippoliti, R A Sturdevant, J I Isenberg, et al.
American Journal of Human Genetics|July 27, 1999
A genome scan for familial combined hyperlipidemia reveals evidence of linkage with a locus on chromosome 11B E Aouizerat, H Allayee, R M Cantor, et al.
Human Molecular Genetics|August 25, 2000
Identification of TNFRSF1B as a novel modifier gene in familial combined hyperlipidemiaJ M Geurts, R G Janssen, M M van Greevenbroek, et al.
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