Showing results (281-290 of 416) with videos related to
Sort By:
Pageof 42
American Journal of Medical Genetics|October 1, 1989
Familial Mediterranean fever in Armenians: autosomal recessive inheritance with high gene frequencyD B Rogers, M Shohat, G M Petersen, et al.Advances in Experimental Medicine and Biology|January 1, 1986
Uridine monophosphate kinase and susceptibility to invasive Haemophilus influenzae type B diseaseG M Petersen, D R Silimperi, E M Scott, et al.The Journal of Pediatrics|December 1, 1977
Heterogeneity of nonlethal severe short-limbed dwarfismG Romeo, J Zonana, D L Rimoin, et al.American Journal of Human Genetics|June 23, 1998
Localization of a multiple synostoses-syndrome disease gene to chromosome 17q21-22D Krakow, K Reinker, B Powell, et al.Genetic Epidemiology. Supplement|January 1, 1986
HLA haplotype sharing and proband genotype in IDDMJ I Rotter, C M Vadheim, G M Petersen, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 17, 2001
A familial risk profile for osteoporosisL B Henderson, J S Adams, D R Goldstein, et al.Journal of Medical Genetics|February 1, 1992
Sensorineural deafness inherited as a tissue specific mitochondrial disorderL Jaber, M Shohat, X Bu, et al.Circulation|December 31, 1997
Association between serum amyloid A proteins and coronary artery disease: evidence from two distinct arteriosclerotic processesA I Fyfe, L S Rothenberg, F C DeBeer, et al.Proceedings of the Association of American Physicians|May 23, 1998
The genetic basis of systemic lupus erythematosusB P Tsao, R M Cantor, K C Kalunian, et al.Journal of Thrombosis and Haemostasis : JTH|March 18, 2014
Associations of pentraxin 3 with cardiovascular disease: the Multi-Ethnic Study of AtherosclerosisN S Jenny, R S Blumenthal, R A Kronmal, et al.Pageof 42