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4. Intrauterine phenotype features of fetuses with Williams-Beuren syndrome and literature review. Yuan M; Deng L; Yang Y; Sun L Ann Hum Genet; 2020 Mar; 84(2):169-176. PubMed ID: 31711272 [TBL] [Abstract][Full Text] [Related]
5. Williams-Beuren syndrome: the prenatal phenotype. Popowski T; Vialard F; Leroy B; Bault JP; Molina-Gomes D Am J Obstet Gynecol; 2011 Dec; 205(6):e6-8. PubMed ID: 22000898 [TBL] [Abstract][Full Text] [Related]
6. Antenatal ultrasound features of isolated recurrent copy number variation in 7q11.23 (Williams syndrome and 7q11.23 duplication syndrome). Courdier C; Boudjarane J; Malan V; Muti C; Sperelakis-Beedham B; Odent S; Jaillard S; Quelin C; Le Caignec C; Patat O; Dubucs C; Julia S; Schluth-Bolard C; Goumy C; Redon S; Gaillard JB; Huynh MT; Dupont C; Tabet AC; Cogan G; Vialard F; Dard R; Jedraszak G; Jobic F; Lefebvre M; Quenum G; Inai S; Rama M; Sauvestre F; Coatleven F; Thomas J; Rooryck C Prenat Diagn; 2023 Jun; 43(6):734-745. PubMed ID: 36914926 [TBL] [Abstract][Full Text] [Related]
7. [Genetic and prenatal diagnosis for four families with Williams-Beuren syndrome]. Liu Y; Xu ZY; Wu WQ; Luo FW; Xie JS Zhongguo Dang Dai Er Ke Za Zhi; 2015 Dec; 17(12):1267-72. PubMed ID: 26695662 [TBL] [Abstract][Full Text] [Related]
8. Anterior segment dysgenesis associated with Williams-Beuren syndrome: a case report and review of the literature. Todorova MG; Grieshaber MC; Cámara RJ; Miny P; Palmowski-Wolfe AM BMC Ophthalmol; 2014 May; 14():70. PubMed ID: 24885071 [TBL] [Abstract][Full Text] [Related]
9. Prenatal ultrasound diagnosis of congenital vertical talus. Xiu Y; Wang Y; He F; Zhang Y; Wang Y; Sun W; Wang B; Chen L J Matern Fetal Neonatal Med; 2023 Dec; 36(1):2192323. PubMed ID: 36948222 [TBL] [Abstract][Full Text] [Related]
10. [Congenital heart disease and nuchal translucency with normal karyotype. Report of 3 cases]. Gicquel JM; Potier A; Camillieri JF; Grinneiser D; Rouault F J Gynecol Obstet Biol Reprod (Paris); 1998 Oct; 27(6):625-8. PubMed ID: 9854228 [TBL] [Abstract][Full Text] [Related]
11. Prenatal diagnosis of Williams-Beuren syndrome by ultrasound and chromosomal microarray analysis. Huang R; Zhou H; Fu F; Li R; Lei T; Li Y; Cheng K; Wang Y; Yang X; Li L; Jing X; Zhang Y; Li F; Li D; Liao C Mol Cytogenet; 2022 Jun; 15(1):27. PubMed ID: 35765027 [TBL] [Abstract][Full Text] [Related]
12. The Prenatal Diagnosis of Seven Fetuses with 7q11.23 Microdeletion or Microduplication. Dang Y; Wan S; Zheng Y; Song T; Li C; Li Y; Zhang J Fetal Pediatr Pathol; 2020 Aug; 39(4):269-276. PubMed ID: 31402733 [No Abstract] [Full Text] [Related]
13. Echocardiographic findings in patients with Williams-Beuren syndrome. Scheiber D; Fekete G; Urban Z; Tarjan I; Balaton G; Kosa L; Nagy K; Vajo Z Wien Klin Wochenschr; 2006 Sep; 118(17-18):538-42. PubMed ID: 17009066 [TBL] [Abstract][Full Text] [Related]
14. [Genetic diagnosis and noninvasive prenatal testing of a family with Williams-Beuren syndrome]. Zhao Y; Pang H; Feng X; Xiang Y; Gao M; Hua J; Tong D; Wu L; Sun H Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Mar; 36(3):263-266. PubMed ID: 30835361 [TBL] [Abstract][Full Text] [Related]
15. A novel dNTP-limited PCR and HRM assay to detect Williams-Beuren syndrome. Zhang L; Zhang X; You G; Yu Y; Fu Q Clin Chim Acta; 2018 Jun; 481():171-176. PubMed ID: 29550276 [TBL] [Abstract][Full Text] [Related]
16. Genotype-phenotype correlation and the size of microdeletion or microduplication of 7q11.23 region in patients with Williams-Beuren syndrome. Ghaffari M; Tahmasebi Birgani M; Kariminejad R; Saberi A Ann Hum Genet; 2018 Nov; 82(6):469-476. PubMed ID: 30155880 [TBL] [Abstract][Full Text] [Related]
17. [Clinical aspects and genetics of Williams-Beuren syndrome. Clinical and molecular genetic study of 44 patients with suspected Williams-Beuren syndrome]. von Beust G; Laccone FA; del Pilar Andrino M; Wessel A Klin Padiatr; 2000; 212(6):299-307. PubMed ID: 11190824 [TBL] [Abstract][Full Text] [Related]
18. Rare genomic rearrangement in a boy with Williams-Beuren syndrome associated to XYY syndrome and intriguing behavior. Dutra RL; Piazzon FB; Zanardo ÉA; Costa TV; Montenegro MM; Novo-Filho GM; Dias AT; Nascimento AM; Kim CA; Kulikowski LD Am J Med Genet A; 2015 Dec; 167A(12):3197-203. PubMed ID: 26420477 [TBL] [Abstract][Full Text] [Related]
19. Detection of deletions at 7q11.23 in Williams-Beuren syndrome by polymorphic markers. Dutra RL; Pieri Pde C; Teixeira AC; Honjo RS; Bertola DR; Kim CA Clinics (Sao Paulo); 2011; 66(6):959-64. PubMed ID: 21808859 [TBL] [Abstract][Full Text] [Related]
20. Prenatal diagnosis of Williams syndrome based on ultrasound signs. Krzeminska D; Steinfeld C; Cloez JL; Vibert M; Chery M; Menzies D; Gilbert-Dussardier B Prenat Diagn; 2009 Jul; 29(7):710-2. PubMed ID: 19340838 [No Abstract] [Full Text] [Related] [Next] [New Search]