223 related articles for article (PubMed ID: 9637430)
1. Delineation of the common critical region in Williams syndrome and clinical correlation of growth, heart defects, ethnicity, and parental origin.
Wu YQ; Sutton VR; Nickerson E; Lupski JR; Potocki L; Korenberg JR; Greenberg F; Tassabehji M; Shaffer LG
Am J Med Genet; 1998 Jun; 78(1):82-9. PubMed ID: 9637430
[TBL] [Abstract][Full Text] [Related]
2. Molecular definition of the chromosome 7 deletion in Williams syndrome and parent-of-origin effects on growth.
Pérez Jurado LA; Peoples R; Kaplan P; Hamel BC; Francke U
Am J Hum Genet; 1996 Oct; 59(4):781-92. PubMed ID: 8808592
[TBL] [Abstract][Full Text] [Related]
3. Strong correlation of elastin deletions, detected by FISH, with Williams syndrome: evaluation of 235 patients.
Lowery MC; Morris CA; Ewart A; Brothman LJ; Zhu XL; Leonard CO; Carey JC; Keating M; Brothman AR
Am J Hum Genet; 1995 Jul; 57(1):49-53. PubMed ID: 7611295
[TBL] [Abstract][Full Text] [Related]
4. Complete physical map of the common deletion region in Williams syndrome and identification and characterization of three novel genes.
Meng X; Lu X; Li Z; Green ED; Massa H; Trask BJ; Morris CA; Keating MT
Hum Genet; 1998 Nov; 103(5):590-9. PubMed ID: 9860302
[TBL] [Abstract][Full Text] [Related]
5. Williams syndrome: use of chromosomal microdeletions as a tool to dissect cognitive and physical phenotypes.
Tassabehji M; Metcalfe K; Karmiloff-Smith A; Carette MJ; Grant J; Dennis N; Reardon W; Splitt M; Read AP; Donnai D
Am J Hum Genet; 1999 Jan; 64(1):118-25. PubMed ID: 9915950
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. GTF2I hemizygosity implicated in mental retardation in Williams syndrome: genotype-phenotype analysis of five families with deletions in the Williams syndrome region.
Morris CA; Mervis CB; Hobart HH; Gregg RG; Bertrand J; Ensing GJ; Sommer A; Moore CA; Hopkin RJ; Spallone PA; Keating MT; Osborne L; Kimberley KW; Stock AD
Am J Med Genet A; 2003 Nov; 123A(1):45-59. PubMed ID: 14556246
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Deletions of the elastin gene at 7q11.23 occur in approximately 90% of patients with Williams syndrome.
Nickerson E; Greenberg F; Keating MT; McCaskill C; Shaffer LG
Am J Hum Genet; 1995 May; 56(5):1156-61. PubMed ID: 7726172
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Elastin region deletions in Williams syndrome.
Zhang J; Kumar A; Roux K; Williams CA; Wallace MR
Genet Test; 1999; 3(4):357-9. PubMed ID: 10627943
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. 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]
15. The human calcitonin receptor gene (CALCR) at 7q21.3 is outside the deletion associated with the Williams syndrome.
Pérez Jurado LA; Li X; Francke U
Cytogenet Cell Genet; 1995; 70(3-4):246-9. PubMed ID: 7789182
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. 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]
19. 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]
20. 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]
[Next] [New Search]
