188 related articles for article (PubMed ID: 35765027)
1. 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]
2. 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]
3. Prenatal phenotype features and genetic etiology of the Williams-Beuren syndrome and literature review.
Wang Y; Liu C; Hu R; Geng J; Lu J; Zhao X; Xiong Y; Wu J; Yin A
Front Pediatr; 2023; 11():1141665. PubMed ID: 37009295
[TBL] [Abstract][Full Text] [Related]
4. Prenatal diagnosis of 7q11.23 microdeletion: Two cases report and literature review.
Lv X; Yang X; Li L; Yue F; Zhang H; Wang R
Medicine (Baltimore); 2023 Oct; 102(43):e34852. PubMed ID: 37904428
[TBL] [Abstract][Full Text] [Related]
5. [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]
6. [Diagnosis of a case with Williams-Beuren syndrome with nephrocalcinosis using chromosome microarray analysis].
Jin SJ; Liu M; Long WJ; Luo XP
Zhonghua Er Ke Za Zhi; 2016 Dec; 54(12):941-945. PubMed ID: 27938597
[No Abstract] [Full Text] [Related]
7. Differing Microdeletion Sizes and Breakpoints in Chromosome 7q11.23 in Williams-Beuren Syndrome Detected by Chromosomal Microarray Analysis.
Li L; Huang L; Luo Y; Huang X; Lin S; Fang Q
Mol Syndromol; 2016 Feb; 6(6):268-75. PubMed ID: 27022327
[TBL] [Abstract][Full Text] [Related]
8. New findings concerning cardiovascular manifestations emerging from long-term follow-up of 150 patients with the Williams-Beuren-Beuren syndrome.
Del Pasqua A; Rinelli G; Toscano A; Iacobelli R; Digilio C; Marino B; Saffirio C; Mondillo S; Pasquini L; Sanders SP; de Zorzi A
Cardiol Young; 2009 Dec; 19(6):563-7. PubMed ID: 19941695
[TBL] [Abstract][Full Text] [Related]
9. [Prenatal diagnosis for a pregnant woman affected with Williams-Beuren syndrome].
Xi N; Zhang Z; Wang X; Sun L; Song X; Li S; Liu S
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 May; 36(5):495-497. PubMed ID: 31030442
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Cardiovascular spectrum in Williams-Beuren syndrome: the Mexican experience in 40 patients.
De Rubens Figueroa J; Rodríguez LM; Hach JL; Del Castillo Ruíz V; Martínez HO
Tex Heart Inst J; 2008; 35(3):279-85. PubMed ID: 18941598
[TBL] [Abstract][Full Text] [Related]
12. [Clinical and genetic characteristics of Williams-Beuren syndrome: 2 cases report].
Wang SQ; Yang ZX; Li H
Beijing Da Xue Xue Bao Yi Xue Ban; 2017 Oct; 49(5):899-903. PubMed ID: 29045977
[TBL] [Abstract][Full Text] [Related]
13. Williams-Beuren syndrome in the Hong Kong Chinese population: retrospective study.
Yau EK; Lo IF; Lam ST
Hong Kong Med J; 2004 Feb; 10(1):22-7. PubMed ID: 14967851
[TBL] [Abstract][Full Text] [Related]
14. Computerized Tomography Use in Williams-Beuren Syndrome Aortopathy.
Kalis NN; Sulaibikh LK; Al Amer SR; Al Amer HY
Heart Views; 2017; 18(1):21-25. PubMed ID: 28584589
[TBL] [Abstract][Full Text] [Related]
15. Congenital heart defects in Williams syndrome.
Yuan SM
Turk J Pediatr; 2017; 59(3):225-232. PubMed ID: 29376566
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Recurrent achalasia in a child with Williams-Beuren syndrome.
Pereza N; Barbarić I; Ostojić S; Cace N; Kapović M
Coll Antropol; 2011 Sep; 35(3):941-4. PubMed ID: 22053584
[TBL] [Abstract][Full Text] [Related]
18. A 1.3-mb 7q11.23 atypical deletion identified in a cohort of patients with williams-beuren syndrome.
Delgado LM; Gutierrez M; Augello B; Fusco C; Micale L; Merla G; Pastene EA
Mol Syndromol; 2013 Mar; 4(3):143-7. PubMed ID: 23653586
[TBL] [Abstract][Full Text] [Related]
19. Renal and urinary findings in 20 patients with Williams-Beuren syndrome diagnosed by fluorescence in situ hybridization (FISH).
Sugayama SM; Koch VH; Furusawa EA; Leone C; Kim CA
Rev Hosp Clin Fac Med Sao Paulo; 2004 Oct; 59(5):266-72. PubMed ID: 15543398
[TBL] [Abstract][Full Text] [Related]
20. Aortopathy in the 7q11.23 microduplication syndrome.
Parrott A; James J; Goldenberg P; Hinton RB; Miller E; Shikany A; Aylsworth AS; Kaiser-Rogers K; Ferns SJ; Lalani SR; Ware SM
Am J Med Genet A; 2015 Feb; 167A(2):363-70. PubMed ID: 25428557
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
