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American Journal of Medical Genetics|January 1, 1979
The Perrault syndrome: autosomal recessive ovarian dysgenesis with facultative, non-sex-limited sensorineural deafnessP D Pallister, J M OpitzBirth Defects Original Article Series|January 1, 1987
The developmental field concept in pediatric pathology--especially with respect to fibular a/hypoplasia and the DiGeorge anomalyJ M Opitz, S O LewinAmerican Journal of Medical Genetics|November 1, 1985
Disequilibrium syndrome in Montana HutteritesP D Pallister, J M OpitzAnnals of Neurology|April 18, 1998
Cerebrospinal fluid homovanillic acid levels in rapid-onset dystonia-parkinsonismA Brashear, I J Butler, K Hyland, et al.Mechanisms of Development|March 23, 2000
Lissencephaly associated mutations suggest a requirement for the PAFAH1B heterotrimeric complex in brain developmentK J Sweeney, G D Clark, A Prokscha, et al.European Journal of Pediatrics|September 1, 1976
A new familial intrauterine growth retardation syndrome the "3-M syndrome"J Spranger, J M Opitz, A NourmandAmerican Journal of Medical Genetics|May 1, 1994
Cholesterol metabolism in the RSH/Smith-Lemli-Opitz syndrome: summary of an NICHD conferenceJ M Opitz, F de la CruzClinical Genetics|March 1, 1976
Familial spastic paraplegia with distal muscle wasting in the Old Order Amish; atypical Troyer syndrome or "new" syndromeG Neuhäuser, C Wiffler, J M OpitzPediatric Neurology|September 1, 1995
Congenital muscular dystrophies: clinical review and proposed classificationE Parano, L Pavone, A Fiumara, et al.American Journal of Human Genetics|March 1, 1991
Clinical and molecular diagnosis of Miller-Dieker syndromeW B Dobyns, C J Curry, H E Hoyme, et al.Pageof 40