223 related articles for article (PubMed ID: 21062444)
1. The use of array-CGH in a cohort of Greek children with developmental delay.
Manolakos E; Vetro A; Kefalas K; Rapti SM; Louizou E; Garas A; Kitsos G; Vasileiadis L; Tsoplou P; Eleftheriades M; Peitsidis P; Orru S; Liehr T; Petersen MB; Thomaidis L
Mol Cytogenet; 2010 Nov; 3():22. PubMed ID: 21062444
[TBL] [Abstract][Full Text] [Related]
2. The clinical benefit of array-based comparative genomic hybridization for detection of copy number variants in Czech children with intellectual disability and developmental delay.
Wayhelova M; Smetana J; Vallova V; Hladilkova E; Filkova H; Hanakova M; Vilemova M; Nikolova P; Gromesova B; Gaillyova R; Kuglik P
BMC Med Genomics; 2019 Jul; 12(1):111. PubMed ID: 31337399
[TBL] [Abstract][Full Text] [Related]
3. Screening of copy number variants in the 22q11.2 region of congenital heart disease patients from the São Miguel Island, Azores, revealed the second patient with a triplication.
Pires R; Pires LM; Vaz SO; Maciel P; Anjos R; Moniz R; Branco CC; Cabral R; Carreira IM; Mota-Vieira L
BMC Genet; 2014 Nov; 15():115. PubMed ID: 25376777
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Confirmation of chromosomal microarray as a first-tier clinical diagnostic test for individuals with developmental delay, intellectual disability, autism spectrum disorders and dysmorphic features.
Battaglia A; Doccini V; Bernardini L; Novelli A; Loddo S; Capalbo A; Filippi T; Carey JC
Eur J Paediatr Neurol; 2013 Nov; 17(6):589-99. PubMed ID: 23711909
[TBL] [Abstract][Full Text] [Related]
6. Use of targeted array-based CGH for the clinical diagnosis of chromosomal imbalance: is less more?
Bejjani BA; Saleki R; Ballif BC; Rorem EA; Sundin K; Theisen A; Kashork CD; Shaffer LG
Am J Med Genet A; 2005 Apr; 134(3):259-67. PubMed ID: 15723295
[TBL] [Abstract][Full Text] [Related]
7. Analysis of Copy Number Variations in Patients with Autism Using Cytogenetic and MLPA Techniques: Report of 16p13.1p13.3 and 10q26.3 Duplications.
Ghasemi Firouzabadi S; Vameghi R; Kariminejad R; Darvish H; Banihashemi S; Firouzkouhi Moghaddam M; Jamali P; Farbod Mofidi Tehrani H; Dehghani H; Raeisoon MR; Narooie-Nejad M; Jamshidi J; Tafakhori A; Sadabadi S; Behjati F
Int J Mol Cell Med; 2016; 5(4):236-245. PubMed ID: 28357200
[TBL] [Abstract][Full Text] [Related]
8. Application of metaphase HR-CGH and targeted Chromosomal Microarray Analyses to genomic characterization of 116 patients with mental retardation and dysmorphic features.
Nowakowska B; Stankiewicz P; Obersztyn E; Ou Z; Li J; Chinault AC; Smyk M; Borg K; Mazurczak T; Cheung SW; Bocian E
Am J Med Genet A; 2008 Sep; 146A(18):2361-9. PubMed ID: 18698622
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. Whole-genome array-CGH for detection of submicroscopic chromosomal imbalances in children with mental retardation.
Thuresson AC; Bondeson ML; Edeby C; Ellis P; Langford C; Dumanski JP; Annerén G
Cytogenet Genome Res; 2007; 118(1):1-7. PubMed ID: 17901693
[TBL] [Abstract][Full Text] [Related]
12. Identification of De Novo and Rare Inherited Copy Number Variants in Children with Syndromic Congenital Heart Defects.
Hussein IR; Bader RS; Chaudhary AG; Bassiouni R; Alquaiti M; Ashgan F; Schulten HJ; Al Qahtani MH
Pediatr Cardiol; 2018 Jun; 39(5):924-940. PubMed ID: 29541814
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Combined 22q11.1-q11.21 deletion with 15q11.2-q13.3 duplication identified by array-CGH in a 6 years old boy.
Manolakos E; Sarri C; Vetro A; Kefalas K; Leze E; Sofocleus C; Kitsos G; Merou K; Kokotas H; Papadopoulou A; Attilakos A; Petersen MB; Kitsiou-Tzeli S
Mol Cytogenet; 2011 Feb; 4(1):6. PubMed ID: 21345209
[TBL] [Abstract][Full Text] [Related]
15. [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]
16. Diagnostic genome profiling in mental retardation.
de Vries BB; Pfundt R; Leisink M; Koolen DA; Vissers LE; Janssen IM; Reijmersdal Sv; Nillesen WM; Huys EH; Leeuw Nd; Smeets D; Sistermans EA; Feuth T; van Ravenswaaij-Arts CM; van Kessel AG; Schoenmakers EF; Brunner HG; Veltman JA
Am J Hum Genet; 2005 Oct; 77(4):606-16. PubMed ID: 16175506
[TBL] [Abstract][Full Text] [Related]
17. Identification of Extremely Rare Pathogenic CNVs by Array CGH in Saudi Children with Developmental Delay, Congenital Malformations, and Intellectual Disability.
Karim S; Hussein IR; Schulten HJ; Alsaedi S; Mirza Z; Al-Qahtani M; Chaudhary A
Children (Basel); 2023 Mar; 10(4):. PubMed ID: 37189911
[TBL] [Abstract][Full Text] [Related]
18. Whole-genome array-CGH identifies novel contiguous gene deletions and duplications associated with developmental delay, mental retardation, and dysmorphic features.
Aradhya S; Manning MA; Splendore A; Cherry AM
Am J Med Genet A; 2007 Jul; 143A(13):1431-41. PubMed ID: 17568414
[TBL] [Abstract][Full Text] [Related]
19. Array-CGH increased the diagnostic rate of developmental delay or intellectual disability in Taiwan.
Lee CL; Lee CH; Chuang CK; Chiu HC; Chen YJ; Chou CL; Wu PS; Chen CP; Lin HY; Lin SP
Pediatr Neonatol; 2019 Aug; 60(4):453-460. PubMed ID: 30581099
[TBL] [Abstract][Full Text] [Related]
20. Analysis of chromosomal aberrations in patients with mental retardation using the array-CGH technique: a single Czech centre experience.
Zrnová E; Vranová V; Slámová I; Gaillyová R; Kuglík P
Folia Biol (Praha); 2011; 57(5):206-15. PubMed ID: 22123463
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
