Janet M. Stewart

Mutations in <i>FGFR1</i> and <i>FGFR2</i> cause familial and sporadic Pfeiffer syndrome

Ute Schell, Andreas Hehr, George Feldman et al. · Human Molecular Genetics · 1995 · 232 citations

Life Sciences, Genetics, Molecular Genetics +12

SUBMUCOUS CLEFT PALATE

R. C. A. Weatherley-White, Chester Y. Sakura, LYNNE D. BRENNER et al. · Plastic & Reconstructive Surgery · 1972 · 157 citations

Dentistry, Oral Surgery, Plastic Surgery +15

Oral–facial–digital syndrome type VI (Váradi syndrome): Further clinical delineation

M. Münke, Donna M. McDonald‐McGinn, Amy Cronister et al. · American Journal of Medical Genetics · 1990 · 97 citations

Medicine, Neurology, Pediatrics +14

Familial XY gonadal dysgenesis.

Juan Chemke, Remy N Carmichael, Janet M. Stewart et al. · Journal of Medical Genetics · 1970 · 61 citations · Full text

Medicine, Hematology, Immunology +10

Familial cerebral cavernous angioma: A gene localized to a 15‐cm interval on chromosome 7q

António Gil‐Nagel, Jan Dubovsky, Kimerly J. Wilcox et al. · Annals of Neurology · 1996 · 60 citations

Life Sciences, Genetics, Molecular Genetics +6