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American Journal of Medical Genetics|November 11, 1996
Familial DiGeorge/velocardiofacial syndrome with deletions of chromosome area 22q11.2: report of five families with a review of the literatureJ Leana-Cox, S Pangkanon, K R Eanet, et al.
Clinical Genetics|September 1, 1994
Complex chromosomal rearrangements: some breakpoints may have cellular adaptive significanceI W Lurie, E A Wulfsberg, G Prabhakar, et al.
American Journal of Medical Genetics|April 23, 1999
OEIS complex (omphalocele-exstrophy-imperforate anus-spinal defects) in monozygotic twinsD H Lee, J R Cottrell, R C Sanders, et al.
Journal of Inherited Metabolic Disease|August 13, 1998
Molecular characterization of a unique patient with epimerase-deficiency galactosaemiaA Alano, S Almashanu, J M Chinsky, et al.
American Journal of Medical Genetics|March 7, 1998
Antenatal diagnosis of lethal skeletal dysplasiasA E Tretter, R C Saunders, C M Meyers, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|November 4, 2000
Human PRRX1 and PRRX2 genes: cloning, expression, genomic localization, and exclusion as disease genes for Nager syndromeR A Norris, K K Scott, C S Moore, et al.
Annals of Epidemiology|July 17, 2001
A case-control study of nonsyndromic oral clefts in MarylandT H Beaty, H Wang, J B Hetmanski, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|November 5, 1997
Testing for interaction between maternal smoking and TGFA genotype among oral cleft cases born in Maryland 1992-1996T H Beaty, N E Maestri, J B Hetmanski, et al.
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