AAAAAA

   
Results: 1-12 |
Results: 12
Weaver syndrome with neuroblastoma and cardiovascular anomalies
Authors: Huffman, C McCandless, D Jasty, R Matloub, J Robinson, HB Weaver, DD Cohen, MM
Citation: C. Huffman et al., Weaver syndrome with neuroblastoma and cardiovascular anomalies, AM J MED G, 99(3), 2001, pp. 252-255
Distal 13q deletion syndrome and the VACTERL association: Case report, literature review, and possible implications
Authors: Walsh, LE Vance, GH Weaver, DD
Citation: Le. Walsh et al., Distal 13q deletion syndrome and the VACTERL association: Case report, literature review, and possible implications, AM J MED G, 98(2), 2001, pp. 137-144
Partial urorectal septum malformation sequence: A report of 25 cases
Authors: Wheeler, PG Weaver, DD
Citation: Pg. Wheeler et Dd. Weaver, Partial urorectal septum malformation sequence: A report of 25 cases, AM J MED G, 103(2), 2001, pp. 99-105
Familial choanal atresia with maxillary hypoplasia, prognathism, and hypodontia
Authors: Ramos-Arroyo, MA Valiente, A Rodriguez-Toral, E Alonso, AM Moreno, S Weaver, DD
Citation: Ma. Ramos-arroyo et al., Familial choanal atresia with maxillary hypoplasia, prognathism, and hypodontia, AM J MED G, 95(3), 2000, pp. 237-240
Hypogonadism and CHARGE association
Authors: Wheeler, PG Quigley, CA Sadeghi-Nejad, A Weaver, DD
Citation: Pg. Wheeler et al., Hypogonadism and CHARGE association, AM J MED G, 94(3), 2000, pp. 228-231
Exclusion of the branchio-oto-renal syndrome locus (EYA1) from patients with branchio-oculo-facial syndrome. (vol 91, pg 387, 2000)
Authors: Lin, AE Semina, EV Daack-Hirsch, S Roeder, ER Curry, CJR Rosenbaum, K Weaver, DD Murray, JC
Citation: Ae. Lin et al., Exclusion of the branchio-oto-renal syndrome locus (EYA1) from patients with branchio-oculo-facial syndrome. (vol 91, pg 387, 2000), AM J MED G, 93(2), 2000, pp. 169-169
Exclusion of the branchio-oto-renal syndrome locus (EYA1) from patients with branchio-oculo-facial syndrome
Authors: Lin, AE Semina, EV Daack-Hirsch, S Roeder, ER Curry, CJR Rosenbaum, K Weaver, DD Murray, JC
Citation: Ae. Lin et al., Exclusion of the branchio-oto-renal syndrome locus (EYA1) from patients with branchio-oculo-facial syndrome, AM J MED G, 91(5), 2000, pp. 387-390
Minimum guidelines for the delivery of prenatal genetics services
Authors: Sommer, A Lubinsky, M Cichon, M Gilpin, NNS Weaver, DD Ahrens, MJ Hagen, VLM Rinehart, PM
Citation: A. Sommer et al., Minimum guidelines for the delivery of prenatal genetics services, GENET MED, 1(5), 1999, pp. 233-234
Mild autosomal dominant hypophosphatasia: In utero presentation in two families
Authors: Moore, CA Curry, CJR Henthorn, PS Smith, JK Smith, JC O'Lague, P Coburn, SP Weaver, DD Whyte, MP
Citation: Ca. Moore et al., Mild autosomal dominant hypophosphatasia: In utero presentation in two families, AM J MED G, 86(5), 1999, pp. 410-415
Bone mineral density and laboratory evaluation of a type II autosomal dominant osteopetrosis carrier
Authors: Takacs, I Cooper, H Weaver, DD Econs, MJ
Citation: I. Takacs et al., Bone mineral density and laboratory evaluation of a type II autosomal dominant osteopetrosis carrier, AM J MED G, 85(1), 1999, pp. 9-12
Genitourinary anomalies in the charge association
Authors: Ragan, DC Casale, AJ Rink, RC Cain, MP Weaver, DD
Citation: Dc. Ragan et al., Genitourinary anomalies in the charge association, J UROL, 161(2), 1999, pp. 622-625
De novo 10q22 interstitial deletion
Authors: Cook, L Weaver, DD Hartsfield, JK Vance, GH
Citation: L. Cook et al., De novo 10q22 interstitial deletion, J MED GENET, 36(1), 1999, pp. 71-72
Risultati: 1-12 |