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Clinical Genetics|June 1, 1985
Congenital contractural arachnodactyly. Report of four additional families and review of literatureM A Ramos Arroyo, D D Weaver, R K BealsAmerican Journal of Medical Genetics|June 22, 1999
Bone mineral density and laboratory evaluation of a type II autosomal dominant osteopetrosis carrierI Takacs, H Cooper, D D Weaver, et al.American Journal of Medical Genetics|February 15, 1993
Otopalatodigital syndrome type II associated with omphalocele: report of three casesK Young, C K Barth, C Moore, et al.Human Genetics|January 1, 1983
Dicentric chromosome 13 and centromere inactivationS Schwartz, C G Palmer, D D Weaver, et al.Pediatrics|December 1, 1991
Weaver syndrome: a case without early overgrowth and review of the literatureM A Ramos-Arroyo, D D Weaver, E R BanksJournal of Medical Genetics|October 1, 1977
Maxillofacial dysostosisV Escobar, J Eastman, D Weaver, et al.International Journal of Oral Surgery|December 1, 1984
Oral gonococcal infectionV Escobar, A G Farman, R N ArmHuman Heredity|January 1, 1979
Genetic structure of the Queckchi Indians. Dental microdifferentiationV Escobar, P M Conneally, K W KangAmerican Journal of Medical Genetics|February 1, 1984
In utero brain destruction resulting in collapse of the fetal skull, microcephaly, scalp rugae, and neurologic impairment: the fetal brain disruption sequenceL J Russell, D D Weaver, M J Bull, et al.American Journal of Diseases of Children (1960)|October 1, 1981
Microcephaly, microphthalmia, falciform retinal folds, and blindness. A new syndromeA L Jarmas, D D Weaver, F D Ellis, et al.Pageof 12