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American Journal of Medical Genetics|April 29, 1998
Lethal syndrome of skeletal dysplasia and progressive central nervous system degenerationM Khosravi, D D Weaver, M J Bull, et al.American Journal of Diseases of Children (1960)|September 1, 1987
Urorectal septum malformation sequence. Report of six cases and embryological analysisL F Escobar, D D Weaver, D Bixler, et al.American Journal of Medical Genetics|August 1, 1990
Bone dysplasias: the prenatal diagnostic challengeL F Escobar, D Bixler, D D Weaver, et al.American Journal of Diseases of Children (1960)|May 1, 1983
Epidermolysis bullosa--pyloric atresia. An autosomal recessive syndromeM J Bull, A L Norins, D D Weaver, et al.Journal of Craniofacial Genetics and Developmental Biology|January 1, 1990
A morphometric analysis of the fetal craniofacies by ultrasound: fetal cephalometryL F Escobar, D Bixler, L M Padilla, et al.American Journal of Medical Genetics|August 15, 1994
Molecular cytogenetic determination of a deletion/duplication of 1q that results in a trisomy 18 syndrome-like phenotypeR Mewar, W Harrison, D D Weaver, et al.American Journal of Medical Genetics|October 1, 1983
Hirschsprung disease: etiologic implications of unsuccessful prenatal diagnosisA L Jarmas, D D Weaver, L M Padilla, et al.The Journal of Urology|January 23, 1999
Genitourinary anomalies in the CHARGE associationD C Ragan, A J Casale, R C Rink, et al.The Journal of Clinical Investigation|April 1, 1984
A mutation that causes lability of the androgen receptor under conditions that normally promote transformation to the DNA-binding stateW J Kovacs, J E Griffin, D D Weaver, et al.Clinical Genetics|August 1, 1988
Neural tube defects and omphalocele in trisomy 18C A Moore, J P Harmon, L M Padilla, et al.Pageof 8