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Pediatrics|August 1, 1989
Selected midline defect associations: a population studyM J Khoury, J F Cordero, J Mulinare, et al.
American Journal of Medical Genetics|December 18, 1996
Autosomal recessive severe dwarfism in a Sicilian girl: a new form of osteodysplastic primordial dwarfism?G Corsello, A Albanese, M Piccione, et al.
American Journal of Medical Genetics. Part A|January 11, 2003
Apparent encephalocele in twin fetus papyraceus with twin-reversal arterial perfusionEnid Gilbert-Barness, John M Opitz, Gabriel Chamyan, et al.
Zeitschrift Fur Kinderheilkunde|July 1, 1975
Syndrome of mental retardation, seizures, hypotonic cerebral palsy and megalocorneae, recessively inheritedG Neuhäuser, E G Kaveggia, T D France, et al.
Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|December 8, 2009
Audio based surveillance forcognitive assistance using a CMT microphone within socially assistive technologyJ E Rougui, D Istrate, W Souidene, et al.
American Journal of Medical Genetics|August 3, 2001
Megacystis-microcolon-intestinal hypoperistalsis syndrome and aganglionosis in trisomy 18G Chamyan, D Debich-Spicer, J M Opitz, et al.
American Journal of Medical Genetics|November 1, 1985
Hutterite cerebro-osteo-nephrodysplasia: autosomal recessive trait in a Lehrerleut Hutterite family from MontanaJ M Opitz, R B Lowry, T M Holmes, et al.
Avian Pathology : Journal of the W.V.P.A|January 1, 1982
A myopathy associated with protozoan schizonts in chickens in commercial farms in peninsular MalaysiaH M Opitz, H J Jakob, E Wiensenhuetter, et al.
European Journal of Pediatrics|March 18, 1977
A biologic and genetic study of 40 cases of severe pure mental retardationJ M Becker, E G Kaveggia, E Pendleton, et al.
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