274 related articles for article (PubMed ID: 33098373)
21. Delineation of 7q11.2 deletions associated with Williams-Beuren syndrome and mapping of a repetitive sequence to within and to either side of the common deletion.
Robinson WP; Waslynka J; Bernasconi F; Wang M; Clark S; Kotzot D; Schinzel A
Genomics; 1996 May; 34(1):17-23. PubMed ID: 8661020
[TBL] [Abstract][Full Text] [Related]
22. Identification of a putative transcription factor gene (WBSCR11) that is commonly deleted in Williams-Beuren syndrome.
Osborne LR; Campbell T; Daradich A; Scherer SW; Tsui LC
Genomics; 1999 Apr; 57(2):279-84. PubMed ID: 10198167
[TBL] [Abstract][Full Text] [Related]
23. Williams-Beuren syndrome: phenotypic variability and deletions of chromosomes 7, 11, and 22 in a series of 52 patients.
Joyce CA; Zorich B; Pike SJ; Barber JC; Dennis NR
J Med Genet; 1996 Dec; 33(12):986-92. PubMed ID: 9004128
[TBL] [Abstract][Full Text] [Related]
24. Constitutional and somatic deletions of the Williams-Beuren syndrome critical region in non-Hodgkin lymphoma.
Guenat D; Quentin S; Rizzari C; Lundin C; Coliva T; Edery P; Fryssira H; Bermont L; Ferrand C; Soulier J; Borg C; Rohrlich PS
J Hematol Oncol; 2014 Nov; 7():82. PubMed ID: 25388916
[TBL] [Abstract][Full Text] [Related]
25. FISH analysis in both classical and atypical cases of Williams-Beuren syndrome.
Hou JW; Wang JK; Wang TR
Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1998; 39(6):398-403. PubMed ID: 9926515
[TBL] [Abstract][Full Text] [Related]
26. Pulmonary function and emphysema in Williams-Beuren syndrome.
Wan ES; Pober BR; Washko GR; Raby BA; Silverman EK
Am J Med Genet A; 2010 Mar; 152A(3):653-6. PubMed ID: 20186780
[TBL] [Abstract][Full Text] [Related]
27. Williams-Beuren Syndrome and Burkitt Leukemia.
Zhukova N; Naqvi A
J Pediatr Hematol Oncol; 2013 Jan; 35(1):e30-2. PubMed ID: 23018576
[TBL] [Abstract][Full Text] [Related]
28. Investigation of deletions at 7q11.23 in 44 patients referred for Williams-Beuren syndrome, using FISH and four DNA polymorphisms.
Brøndum-Nielsen K; Beck B; Gyftodimou J; Hørlyk H; Liljenberg U; Petersen MB; Pedersen W; Petersen MB; Sand A; Skovby F; Stafanger G; Zetterqvist P; Tommerup N
Hum Genet; 1997 Jan; 99(1):56-61. PubMed ID: 9003495
[TBL] [Abstract][Full Text] [Related]
29. Familial Williams-Beuren syndrome showing varying clinical expression.
Pankau R; Siebert R; Kautza M; Schneppenheim R; Gosch A; Wessel A; Partsch CJ
Am J Med Genet; 2001 Feb; 98(4):324-9. PubMed ID: 11170076
[TBL] [Abstract][Full Text] [Related]
30. [Atypical deletions in Williams-Beuren syndrome].
Ramírez-Velazco A; Domínguez-Quezada MG
Rev Med Inst Mex Seguro Soc; 2017; 55(5):615-620. PubMed ID: 29193944
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. Growth assessment in children with Williams-Beuren syndrome: a systematic review.
de Sousa Lima Strafacci A; Fernandes Camargo J; Bertapelli F; Guerra Júnior G
J Appl Genet; 2020 May; 61(2):205-212. PubMed ID: 32157657
[TBL] [Abstract][Full Text] [Related]
33. Molecular and phenotypic characterization of atypical Williams-Beuren syndrome.
Euteneuer J; Carvalho CM; Kulkarni S; Vineyard M; Grady RM; Lupski JR; Shinawi M
Clin Genet; 2014 Nov; 86(5):487-91. PubMed ID: 24246242
[TBL] [Abstract][Full Text] [Related]
34. Anxious, hypoactive phenotype combined with motor deficits in Gtf2ird1 null mouse model relevant to Williams syndrome.
Schneider T; Skitt Z; Liu Y; Deacon RM; Flint J; Karmiloff-Smith A; Rawlins JN; Tassabehji M
Behav Brain Res; 2012 Aug; 233(2):458-73. PubMed ID: 22652393
[TBL] [Abstract][Full Text] [Related]
35. [Genetic analysis of a child with atypical Williams-Beuren syndrome presenting as supravalvular aortic stenosis].
Wu D; Zhang M; Gao Y; Huo X; Xiao H; Zhang Q; Kang B; Wang X; Liao S
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Apr; 37(4):475-478. PubMed ID: 32219841
[TBL] [Abstract][Full Text] [Related]
36. A physical map, including a BAC/PAC clone contig, of the Williams-Beuren syndrome--deletion region at 7q11.23.
Peoples R; Franke Y; Wang YK; Pérez-Jurado L; Paperna T; Cisco M; Francke U
Am J Hum Genet; 2000 Jan; 66(1):47-68. PubMed ID: 10631136
[TBL] [Abstract][Full Text] [Related]
37. Williams-Beuren syndrome in Mexican patients confirmed by FISH and assessed by aCGH.
Ramírez-Velazco A; Aguayo-Orozco TA; Figuera L; Rivera H; Jave-Suárez L; Aguilar-Lemarroy A; Torres-Reyes LA; Córdova-Fletes C; Barros-Núñez P; Delgadillo-Pérez S; Dávalos-Rodríguez IP; García-Ortiz JE; Domínguez MG
J Genet; 2019 Jun; 98(2):. PubMed ID: 31204697
[TBL] [Abstract][Full Text] [Related]
38. Induced chromosome deletion in a Williams-Beuren syndrome mouse model causes cardiovascular abnormalities.
Goergen CJ; Li HH; Francke U; Taylor CA
J Vasc Res; 2011; 48(2):119-29. PubMed ID: 20926892
[TBL] [Abstract][Full Text] [Related]
39. 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]
40. The elastin gene is disrupted in a family with a balanced translocation t(7;16)(q11.23;q13) associated with a variable expression of the Williams-Beuren syndrome.
Duba HC; Doll A; Neyer M; Erdel M; Mann C; Hammerer I; Utermann G; Grzeschik KH
Eur J Hum Genet; 2002 Jun; 10(6):351-61. PubMed ID: 12080386
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
