449 related articles for article (PubMed ID: 16861145)
1. 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]
2. [Williams syndrome without cardiovascular abnormalities].
Cincinnati P; Genuardi M; Rutiloni C
Minerva Pediatr; 1998 Nov; 50(11):467-71. PubMed ID: 10207296
[TBL] [Abstract][Full Text] [Related]
3. Detection of an atypical 7q11.23 deletion in Williams syndrome patients which does not include the STX1A and FZD3 genes.
Botta A; Novelli G; Mari A; Novelli A; Sabani M; Korenberg J; Osborne LR; Digilio MC; Giannotti A; Dallapiccola B
J Med Genet; 1999 Jun; 36(6):478-80. PubMed ID: 10874638
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Identification of genes from a 500-kb region at 7q11.23 that is commonly deleted in Williams syndrome patients.
Osborne LR; Martindale D; Scherer SW; Shi XM; Huizenga J; Heng HH; Costa T; Pober B; Lew L; Brinkman J; Rommens J; Koop B; Tsui LC
Genomics; 1996 Sep; 36(2):328-36. PubMed ID: 8812460
[TBL] [Abstract][Full Text] [Related]
6. [Genetic diagnosis of Williams syndrome].
Urbán Z; Kiss E; Kádár K; Szabolcs J; Csiszár K; Boyd DC; Fekete G
Orv Hetil; 1997 Jul; 138(27):1749-52. PubMed ID: 9273487
[TBL] [Abstract][Full Text] [Related]
7. Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome.
Ewart AK; Morris CA; Atkinson D; Jin W; Sternes K; Spallone P; Stock AD; Leppert M; Keating MT
Nat Genet; 1993 Sep; 5(1):11-6. PubMed ID: 7693128
[TBL] [Abstract][Full Text] [Related]
8. [Williams syndrome: new insights into genetic etiology, pathogenesis and clinical aspects].
van Hagen JM; Govaerts LC; de Coo IF; Gille JJ; Nieuwint AW; Madan K
Ned Tijdschr Geneeskd; 2001 Mar; 145(9):396-400. PubMed ID: 11253493
[TBL] [Abstract][Full Text] [Related]
9. Molecular cytogenetic diagnosis of Williams syndrome.
Hirota H; Matsuoka R; Kimura M; Imamura S; Joh-o K; Ando M; Takao A; Momma K
Am J Med Genet; 1996 Aug; 64(3):473-7. PubMed ID: 8862624
[TBL] [Abstract][Full Text] [Related]
10. [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]
11. Williams syndrome and the elastin gene in Thai patients.
Ruangdaraganon N; Tocharoentanaphol C; Kotchabhakdi N; Khowsathit P
J Med Assoc Thai; 1999 Nov; 82 Suppl 1():S174-8. PubMed ID: 10730539
[TBL] [Abstract][Full Text] [Related]
12. WBSCR14, a putative transcription factor gene deleted in Williams-Beuren syndrome: complete characterisation of the human gene and the mouse ortholog.
de Luis O; Valero MC; Jurado LA
Eur J Hum Genet; 2000 Mar; 8(3):215-22. PubMed ID: 10780788
[TBL] [Abstract][Full Text] [Related]
13. Use of FISH technique in the diagnosis of chromosomal syndromes.
Iqbal MA; Ulmer C; Sakati N
East Mediterr Health J; 1999 Nov; 5(6):1218-24. PubMed ID: 11924115
[TBL] [Abstract][Full Text] [Related]
14. A complete physical contig and partial transcript map of the Williams syndrome critical region.
Hockenhull EL; Carette MJ; Metcalfe K; Donnai D; Read AP; Tassabehji M
Genomics; 1999 Jun; 58(2):138-45. PubMed ID: 10366445
[TBL] [Abstract][Full Text] [Related]
15. A novel human gene FKBP6 is deleted in Williams syndrome.
Meng X; Lu X; Morris CA; Keating MT
Genomics; 1998 Sep; 52(2):130-7. PubMed ID: 9782077
[TBL] [Abstract][Full Text] [Related]
16. Williams syndrome deficits in visual spatial processing linked to GTF2IRD1 and GTF2I on chromosome 7q11.23.
Hirota H; Matsuoka R; Chen XN; Salandanan LS; Lincoln A; Rose FE; Sunahara M; Osawa M; Bellugi U; Korenberg JR
Genet Med; 2003; 5(4):311-21. PubMed ID: 12865760
[TBL] [Abstract][Full Text] [Related]
17. FISH analysis in patients with clinical diagnosis of Williams syndrome.
Elçioglu N; Mackie-Ogilvie C; Daker M; Berry AC
Acta Paediatr; 1998 Jan; 87(1):48-53. PubMed ID: 9510447
[TBL] [Abstract][Full Text] [Related]
18. Interstitial deletion of chromosome 7q in a patient with Williams syndrome and infantile spasms.
Mizugishi K; Yamanaka K; Kuwajima K; Kondo I
J Hum Genet; 1998; 43(3):178-81. PubMed ID: 9747030
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]