421 related articles for article (PubMed ID: 17480035)
1. Array CGH identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardation.
Ullmann R; Turner G; Kirchhoff M; Chen W; Tonge B; Rosenberg C; Field M; Vianna-Morgante AM; Christie L; Krepischi-Santos AC; Banna L; Brereton AV; Hill A; Bisgaard AM; Müller I; Hultschig C; Erdogan F; Wieczorek G; Ropers HH
Hum Mutat; 2007 Jul; 28(7):674-82. PubMed ID: 17480035
[TBL] [Abstract][Full Text] [Related]
2. De novo 16p13.11 microdeletion identified by high-resolution array CGH in a fetus with increased nuchal translucency.
Law LW; Lau TK; Fung TY; Leung TY; Wang CC; Choy KW
BJOG; 2009 Jan; 116(2):339-43. PubMed ID: 19018765
[TBL] [Abstract][Full Text] [Related]
3. 15q duplication associated with autism in a multiplex family with a familial cryptic translocation t(14;15)(q11.2;q13.3) detected using array-CGH.
Koochek M; Harvard C; Hildebrand MJ; Van Allen M; Wingert H; Mickelson E; Holden JJ; Rajcan-Separovic E; Lewis ME
Clin Genet; 2006 Feb; 69(2):124-34. PubMed ID: 16433693
[TBL] [Abstract][Full Text] [Related]
4. Detection of chromosomal imbalances in children with idiopathic mental retardation by array based comparative genomic hybridisation (array-CGH).
Schoumans J; Ruivenkamp C; Holmberg E; Kyllerman M; Anderlid BM; Nordenskjöld M
J Med Genet; 2005 Sep; 42(9):699-705. PubMed ID: 16141005
[TBL] [Abstract][Full Text] [Related]
5. Array-CGH fine mapping of minor and cryptic HR-CGH detected genomic imbalances in 80 out of 590 patients with abnormal development.
Lybaek H; Meza-Zepeda LA; Kresse SH; Høysaeter T; Steen VM; Houge G
Eur J Hum Genet; 2008 Nov; 16(11):1318-28. PubMed ID: 18461090
[TBL] [Abstract][Full Text] [Related]
6. Duplication of 11p14.3-p15.1 in a mentally retarded proband and his mother detected by G-banding and confirmed by high-resolution CGH and BAC FISH.
Wyandt HE; Shim SH; Mark HF; Huang XL; Milunsky JM
Exp Mol Pathol; 2006 Jun; 80(3):262-6. PubMed ID: 16516886
[TBL] [Abstract][Full Text] [Related]
7. Detection of genomic copy number changes in patients with idiopathic mental retardation by high-resolution X-array-CGH: important role for increased gene dosage of XLMR genes.
Froyen G; Van Esch H; Bauters M; Hollanders K; Frints SG; Vermeesch JR; Devriendt K; Fryns JP; Marynen P
Hum Mutat; 2007 Oct; 28(10):1034-42. PubMed ID: 17546640
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. Molecular characterisation of patients with subtelomeric 22q abnormalities using chromosome specific array-based comparative genomic hybridisation.
Koolen DA; Reardon W; Rosser EM; Lacombe D; Hurst JA; Law CJ; Bongers EM; van Ravenswaaij-Arts CM; Leisink MA; van Kessel AG; Veltman JA; de Vries BB
Eur J Hum Genet; 2005 Sep; 13(9):1019-24. PubMed ID: 15986041
[TBL] [Abstract][Full Text] [Related]
11. A cryptic duplication 22q13.31 to qter leads to a distinct phenotype with mental retardation, microcephaly and mild facial dysmorphism.
Peeters H; Vermeesch J; Fryns JP
Genet Couns; 2008; 19(4):365-71. PubMed ID: 19239079
[TBL] [Abstract][Full Text] [Related]
12. Identification and molecular characterization of two novel chromosomal deletions associated with autism.
Chien WH; Gau SS; Wu YY; Huang YS; Fang JS; Chen YJ; Soong WT; Chiu YN; Chen CH
Clin Genet; 2010 Nov; 78(5):449-56. PubMed ID: 20236125
[TBL] [Abstract][Full Text] [Related]
13. Recurrent 16p11.2 microdeletions in autism.
Kumar RA; KaraMohamed S; Sudi J; Conrad DF; Brune C; Badner JA; Gilliam TC; Nowak NJ; Cook EH; Dobyns WB; Christian SL
Hum Mol Genet; 2008 Feb; 17(4):628-38. PubMed ID: 18156158
[TBL] [Abstract][Full Text] [Related]
14. Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder.
Fernandez BA; Roberts W; Chung B; Weksberg R; Meyn S; Szatmari P; Joseph-George AM; Mackay S; Whitten K; Noble B; Vardy C; Crosbie V; Luscombe S; Tucker E; Turner L; Marshall CR; Scherer SW
J Med Genet; 2010 Mar; 47(3):195-203. PubMed ID: 19755429
[TBL] [Abstract][Full Text] [Related]
15. Characterization of 11p14-p12 deletion in WAGR syndrome by array CGH for identifying genes contributing to mental retardation and autism.
Xu S; Han JC; Morales A; Menzie CM; Williams K; Fan YS
Cytogenet Genome Res; 2008; 122(2):181-7. PubMed ID: 19096215
[TBL] [Abstract][Full Text] [Related]
16. A translocation t(6;7)(p11-p12;q22) associated with autism and mental retardation: localization and identification of candidate genes at the breakpoints.
Vincent JB; Choufani S; Horike S; Stachowiak B; Li M; Dill FJ; Marshall C; Hrynchak M; Pewsey E; Ukadike KC; Friedman JM; Srivastava AK; Scherer SW
Psychiatr Genet; 2008 Jun; 18(3):101-9. PubMed ID: 18496206
[TBL] [Abstract][Full Text] [Related]
17. 16p13.11 duplication is a risk factor for a wide spectrum of neuropsychiatric disorders.
Ramalingam A; Zhou XG; Fiedler SD; Brawner SJ; Joyce JM; Liu HY; Yu S
J Hum Genet; 2011 Jul; 56(7):541-4. PubMed ID: 21614007
[TBL] [Abstract][Full Text] [Related]
18. Characterization of an interstitial deletion 6q13-q14.1 in a female with mild mental retardation, language delay and minor dysmorphisms.
Lespinasse J; Gimelli S; Béna F; Antonarakis SE; Ansermet F; Paoloni-Giacobino A
Eur J Med Genet; 2009; 52(1):49-52. PubMed ID: 18992376
[TBL] [Abstract][Full Text] [Related]
19. [Genomic abnormalities in children with mental retardation and autism: the use of comparative genomic hybridization in situ (HRCGH) and molecular karyotyping with DNA-microchips (array CGH)].
Vorsanova SG; Iurov IIu; Kurinnaia OS; Voinova VIu; Iurov IuB
Zh Nevrol Psikhiatr Im S S Korsakova; 2013; 113(8):46-9. PubMed ID: 24077551
[TBL] [Abstract][Full Text] [Related]
20. X chromosome array-CGH for the identification of novel X-linked mental retardation genes.
Bauters M; Van Esch H; Marynen P; Froyen G
Eur J Med Genet; 2005; 48(3):263-75. PubMed ID: 16179222
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
