261 related articles for article (PubMed ID: 20459802)
1. Submicroscopic subtelomeric aberrations in Chinese patients with unexplained developmental delay/mental retardation.
Wu Y; Ji T; Wang J; Xiao J; Wang H; Li J; Gao Z; Yang Y; Cai B; Wang L; Zhou Z; Tian L; Wang X; Zhong N; Qin J; Wu X; Jiang Y
BMC Med Genet; 2010 May; 11():72. PubMed ID: 20459802
[TBL] [Abstract][Full Text] [Related]
2. Identification of chromosome abnormalities in subtelomeric regions by microarray analysis: a study of 5,380 cases.
Shao L; Shaw CA; Lu XY; Sahoo T; Bacino CA; Lalani SR; Stankiewicz P; Yatsenko SA; Li Y; Neill S; Pursley AN; Chinault AC; Patel A; Beaudet AL; Lupski JR; Cheung SW
Am J Med Genet A; 2008 Sep; 146A(17):2242-51. PubMed ID: 18663743
[TBL] [Abstract][Full Text] [Related]
3. Subtelomeric screening in Serbian children with dysmorphic features and unexplained developmental delay/intellectual disabilities.
Damnjanovic T; Cuturilo G; Maksimovic N; Dimitrijevic N; Mitic V; Jekic B; Lukovic L; Bunjevacki V; Varljen T; Dobricic V; Jovanovic I; Kostic V; Novakovic I
Turk J Pediatr; 2015; 57(2):154-60. PubMed ID: 26690596
[TBL] [Abstract][Full Text] [Related]
4. Detection of cryptic subtelomeric chromosome abnormalities and identification of anonymous chromatin using a quantitative multiplex ligation-dependent probe amplification (MLPA) assay.
Northrop EL; Ren H; Bruno DL; McGhie JD; Coffa J; Schouten J; Choo KH; Slater HR
Hum Mutat; 2005 Nov; 26(5):477-86. PubMed ID: 16170807
[TBL] [Abstract][Full Text] [Related]
5. Clinical utility of multiplex ligation-dependent probe amplification technique in identification of aetiology of unexplained mental retardation: a study in 203 Indian patients.
Boggula VR; Shukla A; Danda S; Hariharan SV; Nampoothiri S; Kumar R; Phadke SR
Indian J Med Res; 2014 Jan; 139(1):66-75. PubMed ID: 24604040
[TBL] [Abstract][Full Text] [Related]
6. [Detection of subtelomeric rearrangements in patients with idiopathic mental retardation/developmental delay].
Wu Y; Jiang YW; Wang XZ; Wang HF; Wang JM; Yang YL; Qin J; Zhong N; Wu XR
Zhonghua Er Ke Za Zhi; 2007 Dec; 45(12):906-11. PubMed ID: 18339278
[TBL] [Abstract][Full Text] [Related]
7. Routine chromosomal microarray analysis is necessary in Korean patients with unexplained developmental delay/mental retardation/autism spectrum disorder.
Shin S; Yu N; Choi JR; Jeong S; Lee KA
Ann Lab Med; 2015 Sep; 35(5):510-8. PubMed ID: 26206688
[TBL] [Abstract][Full Text] [Related]
8. An oligonucleotide based array-CGH system for detection of genome wide copy number changes including subtelomeric regions for genetic evaluation of mental retardation.
Toruner GA; Streck DL; Schwalb MN; Dermody JJ
Am J Med Genet A; 2007 Apr; 143A(8):824-9. PubMed ID: 17366576
[TBL] [Abstract][Full Text] [Related]
9. [Multiplex ligation-dependent probe amplification for detecting submicroscopic chromosomal abnormalities in Chinese children with global developmental delay or intellectual disability].
Wang S; Pan H; Pei P; Zheng X; Zhang Y; Ma Y; Bao X; Yang Y; Wu Y; Qi Y
Zhonghua Yi Xue Za Zhi; 2014 Aug; 94(32):2514-8. PubMed ID: 25410923
[TBL] [Abstract][Full Text] [Related]
10. Use of Multiplex Ligation-Dependent Probe Amplification (MLPA) in screening of subtelomeric regions in children with idiopathic mental retardation.
Mandal K; Boggula VR; Borkar M; Agarwal S; Phadke SR
Indian J Pediatr; 2009 Oct; 76(10):1027-31. PubMed ID: 19907935
[TBL] [Abstract][Full Text] [Related]
11. Utility of subtelomeric fluorescent DNA probes for detection of chromosome anomalies in 425 patients.
Jalal SM; Harwood AR; Sekhon GS; Pham Lorentz C; Ketterling RP; Babovic-Vuksanovic D; Meyer RG; Ensenauer R; Anderson MH; Michels VV
Genet Med; 2003; 5(1):28-34. PubMed ID: 12544473
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Diagnosis and fine mapping of a deletion in distal 11q in two Chinese patients with developmental delay.
Ji T; Wu Y; Wang H; Wang J; Jiang Y
J Hum Genet; 2010 Aug; 55(8):486-9. PubMed ID: 20520618
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. [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]
16. Pure subtelomeric microduplications as a cause of mental retardation.
Ruiter EM; Koolen DA; Kleefstra T; Nillesen WM; Pfundt R; de Leeuw N; Hamel BC; Brunner HG; Sistermans EA; de Vries BB
Clin Genet; 2007 Oct; 72(4):362-8. PubMed ID: 17850634
[TBL] [Abstract][Full Text] [Related]
17. Fine-mapping subtelomeric deletions and duplications by comparative genomic hybridization in 42 individuals.
DeScipio C; Spinner NB; Kaur M; Yaeger D; Conlin LK; Ambrosini A; Hu S; Shan S; Krantz ID; Riethman H
Am J Med Genet A; 2008 Mar; 146A(6):730-9. PubMed ID: 18257100
[TBL] [Abstract][Full Text] [Related]
18. Subtelomeric Copy Number Variations: The Importance of 4p/4q Deletions in Patients with Congenital Anomalies and Developmental Disability.
Novo-Filho GM; Montenegro MM; Zanardo ÉA; Dutra RL; Dias AT; Piazzon FB; Costa TV; Nascimento AM; Honjo RS; Kim CA; Kulikowski LD
Cytogenet Genome Res; 2016; 149(4):241-246. PubMed ID: 27665090
[TBL] [Abstract][Full Text] [Related]
19. Subtelomeric analysis detects a familial 10p;12p rearrangement in two relatives with a distinct syndrome.
Battaglia A; Novelli A; Ceccarini C; Bernardini L; Carey JC
Am J Med Genet A; 2007 Jan; 143A(2):184-8. PubMed ID: 17163546
[TBL] [Abstract][Full Text] [Related]
20. [Analysis of copy number variations in 66 children with unexplained mental retardation/developmental delay using chromosomal microarrays].
Li Y; Qiu W; Ye J; Han L; Zhang H; Gu X
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Dec; 31(6):703-7. PubMed ID: 25449071
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
