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American Journal of Medical Genetics|December 4, 1995
Factors which influence the rate of receiving a routine second newborn screening test in Washington StateD L Doyle, M Sanderson, J Bentvelzen, et al.American Journal of Medical Genetics|December 4, 1995
Infant with mos45,x/46,XY/47,XYY/48,XYYY: genetic and clinical findingsJ E Fox, D Blumenthal, W Brock, et al.American Journal of Medical Genetics|December 4, 1995
Partial monosomy of chromosome 1p36.3: characterization of the critical region and delineation of a syndromeO Reish, S A Berry, B HirschAmerican Journal of Medical Genetics|December 4, 1995
Klippel-Trenaunay-Weber syndrome associated with a 5:11 balanced translocationA J Whelan, M S Watson, F D Porter, et al.American Journal of Medical Genetics|December 4, 1995
Linkage between stature and a region on chromosome 20 and analysis of a candidate gene, bone morphogenetic protein 2D B Thompson, V Ossowski, R C Janssen, et al.American Journal of Medical Genetics|December 4, 1995
DMD and BMD in the same family due to distinct mutationsL Morandi, M Mora, S Tedeschi, et al.American Journal of Medical Genetics|December 4, 1995
Hydrocephalus, skeletal anomalies, and mental disturbances in a mother and three daughters: a new syndromeA Ferlini, M Ragno, P Gobbi, et al.American Journal of Medical Genetics|December 4, 1995
Crossover analysis in a British family suggests that Coffin-Lowry syndrome maps to a 3.4-cM interval in Xp22H Bird, A L Collins, C Oley, et al.American Journal of Medical Genetics|December 4, 1995
Lethal syndrome of slender bones, intrauterine fractures, characteristics facial appearance, and cataracts, resembling Hallermann-Streiff syndrome in two sibsN R Dennis, J Fairhurst, I E MooreAmerican Journal of Medical Genetics|November 6, 1995
Autosomal dominant optic nerve colobomas, vesicoureteral reflux, and renal anomaliesL A Schimmenti, M E Pierpont, B L Carpenter, et al.Pageof 854