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American Journal of Medical Genetics. Supplement|January 1, 1986
A new autosomal dominant acrofacial dysostosis syndromeJ F Reynolds, M J Webb, J M OpitzAmerican Journal of Medical Genetics|March 27, 1995
Severe case of Al Awadi/Raas-Rothschild syndrome or new, possibly autosomal recessive facio-skeleto-genital syndromeF Mollica, D Mazzone, G Cimino, et al.Medical and Pediatric Oncology|January 1, 1979
Teratomas in children and young adultsD J Ganick, E F Gilbert, J M OpitzPediatric Clinics of North America|February 1, 1989
The pathologist's perspective of genetic disease. Malformations and dysmorphologyE Gilbert-Barness, J M Opitz, L A BarnessAmerican Journal of Medical Genetics|October 1, 1985
The syndrome of retinal pigmentary degeneration, microcephaly, and severe mental retardation (Mirhosseini-Holmes-Walton syndrome): report of two patientsH M Mendez, G A Paskulin, C VallandroAmerican Journal of Medical Genetics|March 21, 1998
Complete absence or deficiency of one half of the bodyA Carranza, E Gilbert-Barness, F Madrigal, et al.American Journal of Medical Genetics|April 17, 1998
Errors of morphogenesis and developmental field theoryM L Martínez-Frías, J L Frías, J M OpitzAmerican Journal of Medical Genetics|October 1, 1984
Sensorineural deafness in the FG syndrome: report on four new casesG Neri, B Blumberg, P V Miles, et al.American Journal of Medical Genetics|December 14, 1999
Blaschkolinear malformation syndrome in complex trisomy-7 mosaicismE Magenis, M J Webb, B Spears, et al.European Journal of Pediatrics|July 1, 1981
Niemann-Pick disease type C. Pathological, histochemical, ultrastructural and biochemical studiesE F Gilbert, J Callahan, C Viseskul, et al.Pageof 17