34 Publications (Page 2 of 2)
2005
Clinical outcome and follow-up of the first reported case of Russell-Silver syndrome with the unique combination of maternal uniparental heterodisomy 7 and mosaic trisomy 7
Font-Montgomery, Esperanza⋅Zohn, IE⋅Anderson, KV⋅Stone, Kristyne M⋅Weaver, David D⋅Niswander, L⋅Vance, Gail H⋅Das, Soma and Thurston, Virginia C
Birth Defects Research Part A: Clinical and Molecular Teratology, vol. 73, (no. 8), pp. 577-582, 2005. | Journal Article
 
Johnson-McMillin syndrome: report of a new case with novel features.
Cushman, Lisa J⋅Torres Martinez, Wilfredo and Weaver, David D
Birth defects research. Part A, Clinical and molecular teratology, vol. 73, (no. 9), pp. 638-41, 2005/Sep. | Journal Article
 
Vascular-type disruptive defects in fetuses with homozygous alpha-thalassemia: report of two cases and review of the literature.
Adam, M. P.⋅Adam, Margaret L⋅Chueh, Jane T⋅Chueh, J.⋅El-Sayed, Y. Y.⋅El Sayed, Yasser Y⋅Stenzel, Ana⋅Stenzel, A.⋅Vogel, Hannes⋅Voge, H.⋅Weaver, David D⋅Weaver, D. D.⋅Hoyme, H. E. and Hoyme, H. E
Prenatal diagnosis., vol. 25, (no. 12), pp. 1088-96, 2005/Dec. | Journal Article
2004
Clinical and cytogenetic manifestations of subtelomeric aberrations: Report of six cases.
Font-Montgomery, Esperanza⋅Font‐Montgomery, Esperanza⋅Weaver, David D⋅Weaver, David D⋅Walsh, Laurence⋅Walsh, Laurence⋅Christensen, Celanie⋅Christensen, Celanie⋅Thurston, Virginia C and Thurston, Virginia C
Birth defects research. Part A, Clinical and molecular teratology, vol. 70, (no. 6), pp. 408-15, 2004/Jun. | Journal Article
1999
Bone Mineral Density and Laboratory Evaluation of a Type II Autosomal Dominant Osteopetrosis Carrier
Takacs, I.⋅Cooper, H.⋅Weaver, David D and Econs, Michael
American Journal of Medical Genetics, vol. 85, (no. 1), pp. 9-12, 1999. | Journal Article
 
De novo 10q22 interstitial deletion.
Cook, L⋅Weaver, David D⋅Hartsfield, James K and Vance, Gail H
Journal of medical genetics, vol. 36, (no. 1), pp. 71-2, 1999/Jan. | Journal Article
1998
The syndromes of Sotos and Weaver: reports and review.
Opitz, J M⋅Weaver, David D and Reynolds, J F
American journal of medical genetics, vol. 79, (no. 4), pp. 294-304, 1998/Oct/2. | Journal Article
 
Weaver syndrome: autosomal dominant inheritance of the disorder.
Proud, V K⋅Braddock, S R⋅Cook, L and Weaver, David D
American journal of medical genetics, vol. 79, (no. 4), pp. 305-10, 1998/Oct/2. | Journal Article
1995
Cytogenetic and molecular analysis of a ring (21) in a patient with partial trisomy 21 and megakaryocytic leukemia
Palmer, CG⋅Blouin, J-L⋅Bull, MJ⋅Breitfeld, P.⋅Vance, Gail H⋅Van Meter, T.⋅Weaver, David D⋅Heerema, NA⋅Colbern, SG⋅Korenberg, J. R⋅Antonarakis, SE and Chen, X.
American Journal of Medical Genetics Part A, vol. 57, (no. 4), pp. 527-536, 1995. | Journal Article