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American 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 BanksAmerican 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.European Journal of Pediatrics|May 22, 1978
Femoral hypoplasia-unusual facies syndrome, from another viewpointS Gleiser, D D Weaver, V Escobar, 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.Obstetrics and Gynecology|October 1, 1988
Fetal craniofacial morphometrics: in utero evaluation at 16 weeks' gestationL F Escobar, D Bixler, L M Padilla, et al.Journal of Medical Genetics|February 9, 1999
De novo 10q22 interstitial deletionL Cook, D D Weaver, J K Hartsfield, et al.American Journal of Medical Genetics|October 22, 1998
Weaver syndrome: autosomal dominant inheritance of the disorderV K Proud, S R Braddock, L Cook, et al.Pageof 8