S. D. Fernbach

Defects in neural stem cell proliferation and olfaction in Chd7 deficient mice indicate a mechanism for hyposmia in human CHARGE syndrome

Wanda S. Layman, Dyke P. McEwen, Lisa A. Beyer et al. · Human Molecular Genetics · 2009 · 110 citations · Full text

Life Sciences, Genetics, Neuroscience +17

Linkage disequilibrium, cystic fibrosis, and genetic counseling.

Arthur L. Beaudet, G L Feldman, S. D. Fernbach et al. · PubMed · 1989 · 92 citations

Life Sciences, Genetics, Molecular Genetics +16

PTPN11 Mutations in Noonan syndrome type I: detection of recurrent mutations in exons 3 and 13

M. Maheshwari, John W. Belmont, S. D. Fernbach et al. · Human Mutation · 2002 · 90 citations

Life Sciences, Genetics, Molecular Genetics +12

Prenatal diagnosis of cystic fibrosis using linked DNA markers and microvillar intestinal enzyme analysis

J. Edward Spence, GregoryJ. Buffone, C L Rosenbloom et al. · Human Genetics · 1987 · 32 citations

Medicine, Genetics, Molecular Genetics +16

Prenatal diagnosis of cystic fibrosis: microvillar enzymes and DNA analysis compared.

G J Buffone, J. Edward Spence, S. D. Fernbach et al. · Clinical Chemistry · 1988 · 19 citations

Medicine, Maternal Health, Obstetrics +17