James H. Asher

A gene for congenital, recessive deafness DFNB3 maps to the pericentromeric region of chromosome 17

Thomas B. Friedman, Yong Liang, James L. Weber et al. · Nature Genetics · 1995 · 225 citations

Life Sciences, Genetics, Molecular Genetics +11

Apparent Digenic Inheritance of Waardenburg Syndrome Type 2 (WS2) and Autosomal Recessive Ocular Albinism (AROA)

Robert J. Morell, Richard A. Spritz, L. Ho et al. · Human Molecular Genetics · 1997 · 106 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

A frameshift mutation in the HuP2 paired domain of the probable human homolog of murine <i>Pax-3</i> is responsible for Waardenburg syndrome type 1 in an Indonesian family

Robert J. Morell, Thomas B. Friedman, Sukarti Moeljopawiro et al. · Human Molecular Genetics · 1992 · 92 citations

Life Sciences, Genetics, Molecular Genetics +15

PARTHENOGENESIS AND GENETIC VARIABILITY. I. LINKAGE AND INBREEDING ESTIMATIONS IN THE FROG, <i>RANA PIPIENS</i>

George W. Nace, Christina M. Richards, James H. Asher · Genetics · 1970 · 80 citations

Life Sciences, Genetics, Zoology +7

Missense mutation in the paired domain of PAX3 causes craniofacial-deafness-hand syndrome

James H. Asher, Annemarie Sommer, Robert J. Morell et al. · Human Mutation · 1996 · 80 citations

Life Sciences, Genetics, Molecular Genetics +16