197 related articles for article (PubMed ID: 11057222)
1. [Williams syndrome(Williams-Beuren syndrome), elfin face syndrome].
Ehara H
Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):263-5. PubMed ID: 11057222
[No Abstract] [Full Text] [Related]
2. A new case of keratoconus associated with Williams-Beuren syndrome.
Viana MM; Frasson M; Leão LL; Stofanko M; Gonçalves-Dornelas H; Cunha Pda S; de Aguiar MJ
Ophthalmic Genet; 2013 Sep; 34(3):174-7. PubMed ID: 23167938
[TBL] [Abstract][Full Text] [Related]
3. [Williams syndrome].
Kondo I
Nihon Rinsho; 2006 Sep; Suppl 3():440-3. PubMed ID: 17022583
[No Abstract] [Full Text] [Related]
4. Molecular and clinical correlation study of Williams-Beuren syndrome: No evidence of molecular factors in the deletion region or imprinting affecting clinical outcome.
Wang MS; Schinzel A; Kotzot D; Balmer D; Casey R; Chodirker BN; Gyftodimou J; Petersen MB; Lopez-Rangel E; Robinson WP
Am J Med Genet; 1999 Sep; 86(1):34-43. PubMed ID: 10440826
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. Williams-Beuren syndrome: unraveling the mysteries of a microdeletion disorder.
Osborne LR
Mol Genet Metab; 1999 May; 67(1):1-10. PubMed ID: 10329018
[No Abstract] [Full Text] [Related]
8. [Williams syndrome--developmental syndrome's common cardiovascular disorders].
Peippo M; Hiippala A; Raatikka M; Westerlund A; Johansson R; Arvio M; Eronen M
Duodecim; 2001; 117(5):505-12. PubMed ID: 12116777
[No Abstract] [Full Text] [Related]
9. Hemizygous deletion of the syntaxin 1A gene in individuals with Williams syndrome.
Osborne LR; Soder S; Shi XM; Pober B; Costa T; Scherer SW; Tsui LC
Am J Hum Genet; 1997 Aug; 61(2):449-52. PubMed ID: 9311751
[No Abstract] [Full Text] [Related]
10. Actin, cofilin and cognition.
Rosenblatt J; Mitchison TJ
Nature; 1998 Jun; 393(6687):739-40. PubMed ID: 9655388
[No Abstract] [Full Text] [Related]
11. Localization of the human HIP1 gene close to the elastin (ELN) locus on 7q11.23.
Wedemeyer N; Peoples R; Himmelbauer H; Lehrach H; Francke U; Wanker EE
Genomics; 1997 Dec; 46(2):313-5. PubMed ID: 9417924
[No Abstract] [Full Text] [Related]
12. Genetic aspects of supravalvular aortic stenosis.
Morris CA
Curr Opin Cardiol; 1998 May; 13(3):214-9. PubMed ID: 9649945
[TBL] [Abstract][Full Text] [Related]
13. LIM-kinase deleted in Williams syndrome.
Tassabehji M; Metcalfe K; Fergusson WD; Carette MJ; Dore JK; Donnai D; Read AP; Pröschel C; Gutowski NJ; Mao X; Sheer D
Nat Genet; 1996 Jul; 13(3):272-3. PubMed ID: 8673124
[No Abstract] [Full Text] [Related]
14. [Syndromes 5. Williams-Beuren Syndrome].
Hoff M; van Hagen JM; Baart JA; Vissink A
Ned Tijdschr Tandheelkd; 1998 Oct; 105(10):368-9. PubMed ID: 11928452
[TBL] [Abstract][Full Text] [Related]
15. Keratoconus associated with Williams-Beuren syndrome: first case reports.
Pinsard L; Touboul D; Vu Y; Lacombe D; Leger F; Colin J
Ophthalmic Genet; 2010 Dec; 31(4):252-6. PubMed ID: 21067490
[TBL] [Abstract][Full Text] [Related]
16. Assessment of clinical scoring systems for the diagnosis of Williams-Beuren syndrome.
Leme DE; Souza DH; Mercado G; Pastene E; Dias A; Moretti-Ferreira D
Genet Mol Res; 2013 Sep; 12(3):3407-11. PubMed ID: 24065682
[TBL] [Abstract][Full Text] [Related]
17. LIM-kinase1 hemizygosity implicated in impaired visuospatial constructive cognition.
Frangiskakis JM; Ewart AK; Morris CA; Mervis CB; Bertrand J; Robinson BF; Klein BP; Ensing GJ; Everett LA; Green ED; Pröschel C; Gutowski NJ; Noble M; Atkinson DL; Odelberg SJ; Keating MT
Cell; 1996 Jul; 86(1):59-69. PubMed ID: 8689688
[TBL] [Abstract][Full Text] [Related]
18. Autism and Williams syndrome: a case report.
Herguner S; Mukaddes NM
World J Biol Psychiatry; 2006; 7(3):186-8. PubMed ID: 16861145
[TBL] [Abstract][Full Text] [Related]
19. [Clinical characterization, molecular and FISH studies in 80 patients with clinical suspicion of Williams-Beuren syndrome].
Milà M; Carrió A; Sánchez A; Gómez D; Jiménez D; Estivill X; Ballesta F
Med Clin (Barc); 1999 Jun; 113(2):46-9. PubMed ID: 10425618
[TBL] [Abstract][Full Text] [Related]
20. Williams-Beuren syndrome: determination of deletion size using quantitative real-time PCR.
Schubert C; Laccone F
Int J Mol Med; 2006 Nov; 18(5):799-806. PubMed ID: 17016608
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
