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Journal of Medical Genetics|August 1, 1997
Monozygotic twins discordant for Aicardi syndromeT Costa, W Greer, G Rysiecki, et al.
Journal of Intellectual Disability Research : JIDR|December 7, 2011
Caregiver and adult patient perspectives on the importance of a diagnosis of 22q11.2 deletion syndromeG Costain, E W C Chow, P N Ray, et al.
Molecular and Cellular Biology|January 1, 1990
Molecular and functional analysis of the muscle-specific promoter region of the Duchenne muscular dystrophy geneH J Klamut, S B Gangopadhyay, R G Worton, et al.
American Journal of Medical Genetics|May 30, 1998
FGFR2 mutation associated with clinical manifestations consistent with Antley-Bixler syndromeK Chun, J Siegel-Bartelt, D Chitayat, et al.
The EMBO Journal|December 1, 1991
Molecular analysis of X-autosome translocations in females with Duchenne muscular dystrophyS E Bodrug, J J Holden, P N Ray, et al.
Journal of Biomedical Materials Research|May 7, 1998
Inducible nitric oxide synthase messenger RNA levels in hip periprosthetic tissue: a preliminary studyM L Pearson, S B Goodman, P Huie, et al.
Virology|November 1, 1977
The multisite character of host-range mutations in bacteriophage lambdaJ E Shaw, H Bingham, C R Fuerst, et al.
Medical Care|April 1, 1997
Changes over time in the use of do not resuscitate orders and the outcomes of patients receiving themN S Wenger, M L Pearson, K A Desmond, et al.
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