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Genetic Testing|January 11, 2000
Elastin region deletions in Williams syndromeJ Zhang, A Kumar, K Roux, et al.Nature Genetics|September 1, 1995
Benign neurofibromas in type 1 neurofibromatosis (NF1) show somatic deletions of the NF1 geneS D Colman, C A Williams, M R WallaceJournal of Medical Genetics|August 3, 2005
Genetic linkage of a novel autosomal dominant restrictive cardiomyopathy locusJ Zhang, A Kumar, L Kaplan, et al.British Heart Journal|January 1, 1994
Familial atrioventricular septal defect: possible genetic mechanismsA Kumar, C A Williams, B E VictoricaAmerican Journal of Medical Genetics|March 15, 1993
Concurrence of supravalvular aortic stenosis and peripheral pulmonary stenosis in three generations of a family: a form of arterial dysplasiaA Kumar, H J Stalker, C A WilliamsClinical Genetics|April 12, 2001
Clinical and molecular studies of a large family with desmin-associated restrictive cardiomyopathyJ Zhang, A Kumar, H J Stalker, et al.Human Genetics|September 10, 1999
A new hereditary cylindromatosis family associated with CYLD1 on chromosome 16S A Thomson, S A Rasmussen, J Zhang, et al.Human Genetics|December 6, 2001
Supravalvular aortic stenosis: genetic and molecular dissection of a complex mutation in the elastin geneZ Urbán, J Zhang, E C Davis, et al.The New Zealand Medical Journal|August 26, 1981
Acute glomerulonephritis in childhood: a prospective study of hospital admissionsM R WallaceThe New Zealand Medical Journal|January 26, 1983
Serial serum immunoglobulin levels in acute postinfectious glomerulonephritisM R WallacePageof 1,544