Sarah F. Slaney

Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome

Andrew O.M. Wilkie, Sarah F. Slaney, Michael Oldridge et al. · Nature Genetics · 1995 · 925 citations

Mendelian Disorder, Autoimmune Disease, Genetic Disorder +9

Identical mutations in the FGFR2 gene cause both Pfeiffer and Crouzon syndrome phenotypes

Paul Rutland, Louise J. Pulleyn, William Reardon et al. · Nature Genetics · 1995 · 456 citations

Developmental Biology, Mendelian Disorder, Genetic Disorder +8

Differential effects of FGFR2 mutations on syndactyly and cleft palate in Apert syndrome.

Sarah F. Slaney, Michael Oldridge, J A Hurst et al. · PubMed · 1996 · 235 citations

Asymmetry and skin pigmentary anomalies in chromosome mosaicism.

C. Geoffrey Woods, Agnes Bankier, John Curry et al. · Journal of Medical Genetics · 1994 · 151 citations · Full text

Skin Pigmentary Anomalies, Cytogenetics, Genetics +17

Kabuki make-up and Turner syndromes in the same patient

Diana Wellesley, Sarah F. Slaney · Clinical Dysmorphology · 1994 · 34 citations

Down Syndrome, Developmental Biology, Autoimmune Disease +12