Showing results (1-10 of 8) with videos related to
Sort By:
Pageof 1
Prenatal Diagnosis|November 1, 1987
Prenatal diagnosis of a new syndrome: holoprosencephaly with hypokinesiaR P Morse, E Rawnsley, S K Sargent, et al.Prenatal Diagnosis|October 1, 1987
Bilateral renal agenesis in three consecutive siblingsR P Morse, E Rawnsley, H C Crowe, et al.Prenatal Diagnosis|July 1, 1989
Trisomy 20 mosaicism confirmed in a phenotypically normal livebornJ P Park, J B Moeschler, E Rawnsley, et al.American Journal of Human Genetics|November 1, 1975
Human erythrocyte galactokinase and galactose-1-phosphate uridylyltransferase: a population surveyT A Tedesco, K L Miller, B E Rawnsley, et al.Clinical Genetics|July 1, 1990
Autosomal dominant familial spastic paraplegia: report of a large New England familyW C Cooley, E Rawnsley, G Melkonian, et al.American Journal of Human Genetics|November 1, 1975
Galactose tolerance studies of individuals with reduced galactose pathway activityW J Mellman, B E Rawnsley, C W Nichols, et al.American Journal of Human Genetics|May 1, 1977
The Philadelphia variant of galactokinaseT A Tedesco, K L Miller, B E Rawnsley, et al.American Journal of Human Genetics|March 1, 1996
FGFR2 exon IIIa and IIIc mutations in Crouzon, Jackson-Weiss, and Pfeiffer syndromes: evidence for missense changes, insertions, and a deletion due to alternative RNA splicingG A Meyers, D Day, R Goldberg, et al.Pageof 1