79 related articles for article (PubMed ID: 20807304)
1. Subtelomeric rearrangements and copy number variations in people with intellectual disabilities.
Christofolini DM; de Paula Ramos MA; Kulikowski LD; da Silva Bellucco FT; Belangero SI; Brunoni D; Melaragno MI
J Intellect Disabil Res; 2010 Oct; 54(10):938-42. PubMed ID: 20807304
[TBL] [Abstract][Full Text] [Related]
2. Subtelomeric chromosomal rearrangements detected in patients with idiopathic mental retardation and dysmorphic features.
Caliskan MO; Karauzum SB; Mihci E; Tacoy S; Luleci G
Genet Couns; 2005; 16(2):129-38. PubMed ID: 16080292
[TBL] [Abstract][Full Text] [Related]
3. The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation.
Flint J; Wilkie AO; Buckle VJ; Winter RM; Holland AJ; McDermid HE
Nat Genet; 1995 Feb; 9(2):132-40. PubMed ID: 7719339
[TBL] [Abstract][Full Text] [Related]
4. [Multiplex ligation-dependent probe amplification analysis of subtelomeric chromosome rearrangements in children with idiopathic mental retardation].
Li MR; Wang XZ; Yang YL; Zhang YH; Xiong H; Bao XH; Zhong N; Wu XR; Pan H
Zhonghua Yi Xue Za Zhi; 2009 Nov; 89(40):2839-42. PubMed ID: 20137665
[TBL] [Abstract][Full Text] [Related]
5. Prospective screening of patients with unexplained mental retardation using subtelomeric MLPA strongly increases the detection rate of cryptic unbalanced chromosomal rearrangements.
Stegmann AP; Jonker LM; Engelen JJ
Eur J Med Genet; 2008; 51(2):93-105. PubMed ID: 18032123
[TBL] [Abstract][Full Text] [Related]
6. Detection of known and novel genomic rearrangements by array based comparative genomic hybridisation: deletion of ZNF533 and duplication of CHARGE syndrome genes.
Monfort S; Roselló M; Orellana C; Oltra S; Blesa D; Kok K; Ferrer I; Cigudosa JC; Martínez F
J Med Genet; 2008 Jul; 45(7):432-7. PubMed ID: 18413373
[TBL] [Abstract][Full Text] [Related]
7. Screening for subtelomeric rearrangements in 210 patients with unexplained mental retardation using multiplex ligation dependent probe amplification (MLPA).
Koolen DA; Nillesen WM; Versteeg MH; Merkx GF; Knoers NV; Kets M; Vermeer S; van Ravenswaaij CM; de Kovel CG; Brunner HG; Smeets D; de Vries BB; Sistermans EA
J Med Genet; 2004 Dec; 41(12):892-9. PubMed ID: 15591274
[TBL] [Abstract][Full Text] [Related]
8. Chromosomal rearrangements in children with idiopathic mental retardation using subtelomeric fluorescent in situ hybridization.
Cogulu O; Gunduz C; Karaca E; Onay H; Ozkinay C; Ozkinay F
Genet Couns; 2006; 17(3):321-31. PubMed ID: 17100201
[TBL] [Abstract][Full Text] [Related]
9. Evaluation of MLPA for the detection of cryptic subtelomeric rearrangements.
Monfort S; Orellana C; Oltra S; Roselló M; Guitart M; Martínez F
J Lab Clin Med; 2006 Jun; 147(6):295-300. PubMed ID: 16750667
[TBL] [Abstract][Full Text] [Related]
10. Subtelomeric rearrangements in mental retardation: Hacettepe University experience in 130 patients.
Utine GE; Celik T; Alanay Y; Alikaşifoğlu M; Boduroğlu K; Tunçbilek E; Aktaş D
Turk J Pediatr; 2009; 51(3):199-206. PubMed ID: 19817261
[TBL] [Abstract][Full Text] [Related]
11. Subtelomeric deletions detected in patients with idiopathic mental retardation using multiplex ligation-dependent probe amplification (MLPA).
Rooms L; Reyniers E; van Luijk R; Scheers S; Wauters J; Ceulemans B; Van Den Ende J; Van Bever Y; Kooy RF
Hum Mutat; 2004 Jan; 23(1):17-21. PubMed ID: 14695528
[TBL] [Abstract][Full Text] [Related]
12. FISH screening for subtelomeric rearrangements in 219 patients with idiopathic mental retardation and normal karyotype.
Baroncini A; Rivieri F; Capucci A; Croci G; Franchi F; Sensi A; Battaglia P; Aiello V; Calzolari E
Eur J Med Genet; 2005; 48(4):388-96. PubMed ID: 16378923
[TBL] [Abstract][Full Text] [Related]
13. A novel automated strategy for screening cryptic telomeric rearrangements in children with idiopathic mental retardation.
Colleaux L; Rio M; Heuertz S; Moindrault S; Turleau C; Ozilou C; Gosset P; Raoult O; Lyonnet S; Cormier-Daire V; Amiel J; Le Merrer M; Picq M; de Blois MC; Prieur M; Romana S; Cornelis F; Vekemans M; Munnich A
Eur J Hum Genet; 2001 May; 9(5):319-27. PubMed ID: 11378819
[TBL] [Abstract][Full Text] [Related]
14. Copy number variation in regions flanked (or unflanked) by duplicons among patients with developmental delay and/or congenital malformations; detection of reciprocal and partial Williams-Beuren duplications.
Kriek M; White SJ; Szuhai K; Knijnenburg J; van Ommen GJ; den Dunnen JT; Breuning MH
Eur J Hum Genet; 2006 Feb; 14(2):180-9. PubMed ID: 16391556
[TBL] [Abstract][Full Text] [Related]
15. Chromosomal aberrations, subtelomeric defects, and mental retardation.
Baralle D
Lancet; 2001 Jul; 358(9275):7-8. PubMed ID: 11454368
[No Abstract] [Full Text] [Related]
16. Application of a comprehensive subtelomere array in clinical diagnosis of mental retardation.
Kok K; Dijkhuizen T; Swart YE; Zorgdrager H; van der Vlies P; Fehrmann R; te Meerman GJ; Gerssen-Schoorl KB; van Essen T; Sikkema-Raddatz B; Buys CH
Eur J Med Genet; 2005; 48(3):250-62. PubMed ID: 16179221
[TBL] [Abstract][Full Text] [Related]
17. [A study of subtelomeric rearrangements in 300 patients with mental retardation and multiple congenital anomalies: their clinical and molecular characterisation].
Madrigal I; Rodríguez-Revenga L; Costa L; Xunclà M; Sánchez A; Milà M
Rev Neurol; 2010 Oct; 51(8):465-70. PubMed ID: 20925028
[TBL] [Abstract][Full Text] [Related]
18. MLPA vs multiprobe FISH: comparison of two methods for the screening of subtelomeric rearrangements in 50 patients with idiopathic mental retardation.
Palomares M; Delicado A; Lapunzina P; Arjona D; Amiñoso C; Arcas J; Martinez Bermejo A; Fernández L; López Pajares I
Clin Genet; 2006 Mar; 69(3):228-33. PubMed ID: 16542387
[TBL] [Abstract][Full Text] [Related]
19. High frequency of subtelomeric rearrangements in a cohort of 92 patients with severe mental retardation and dysmorphism.
Novelli A; Ceccarini C; Bernardini L; Zuccarello D; Caputo V; Digilio MC; Mingarelli R; Dallapiccola B
Clin Genet; 2004 Jul; 66(1):30-8. PubMed ID: 15200505
[TBL] [Abstract][Full Text] [Related]
20. Genomic copy number analysis in mental retardation: finding the needles in the haystack.
Veltman JA
Eur J Hum Genet; 2007 Jan; 15(1):1-2. PubMed ID: 17047673
[No Abstract] [Full Text] [Related]
[Next] [New Search]