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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.Plastic and Reconstructive Surgery|September 1, 1990
Unilateral duplication of the cerebellar hemisphere and internal, middle, and external ear: a clinical case studyJ M Jackson, A M Sadove, D D Weaver, et al.Clinical Genetics|October 1, 1984
Endocrine and genetic characterization of cousins with male pseudohermaphroditism: evidence that the Lubs phenotype can result from a mutation that alters the structure of the androgen receptorJ D Wilson, B R Carlson, D D Weaver, et al.Journal of Environmental Management|July 2, 2011
A provider-based water planning and management model--WaterSim 4.0--for the Phoenix Metropolitan AreaD A Sampson, V Escobar, M K Tschudi, et al.Clinical Genetics|March 1, 1979
The human X-chromosome and the levels of serum immunoglobulin MV Escobar, L A Corey, D Bixler, et al.Clinical Genetics|November 1, 1976
Interstitial deletion of the long arm of chromosome no. 7 (7q-) in an infant with multiple anomaliesG Higginson, D D Weaver, R E Magenis, et al.Pageof 12