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American Journal of Medical Genetics|October 1, 1993
Short rib-polydactyly syndrome (SRPS) with anencephaly and other central nervous system anomalies: a new type of SRPS or a more severe expression of a known SRPS entity?M L Martínez-Frías, E Bermejo, M Urioste, et al.American Journal of Medical Genetics|October 1, 1993
Schimke immuno-osseous dysplasia: case report and reviewM D Ludman, D E Cole, J F Crocker, et al.American Journal of Medical Genetics|December 1, 1988
Hepatocellular carcinoma in a child with familial Russell-Silver syndromeD Chitayat, J M Friedman, L Anderson, et al.American Journal of Medical Genetics|August 1, 1992
Five years experience of predictive testing for myotonic dystrophy using linked DNA markersW Reardon, J L Floyd, J Myring, et al.American Journal of Medical Genetics|August 1, 1992
Detection of the heteromorphic spectrum of heterochromatin in the human genome by in situ digestion using restriction endonuclease AluIS Luke, R S VermaAmerican Journal of Medical Genetics|August 1, 1992
Microcephaly, lymphedema, and chorioretinal dysplasia: a distinct syndrome?M Feingold, L BartosheskyAmerican Journal of Medical Genetics|August 1, 1992
VACTERL or MURCS association in a girl with neurenteric cyst and identical thoracic malformations in the father: a case of gonosomal mosaicism?K H Orstavik, J Steen-Johnsen, A Foerster, et al.American Journal of Medical Genetics|August 1, 1992
Delayed replication of Xq27 in individuals with the fragile X syndromeT WebbAmerican Journal of Medical Genetics|August 1, 1992
CNS midline anomalies in the Opitz G/BBB syndrome: report on 12 Brazilian patientsM L Guion-Almeida, A Richieri-CostaAmerican Journal of Medical Genetics|August 1, 1992
Branchio-oto-renal syndrome: further delineation of an underdiagnosed syndromeD Chitayat, K A Hodgkinson, M F Chen, et al.Pageof 854