154 related articles for article (PubMed ID: 24497710)
1. Genomic characterization of some Iranian children with idiopathic mental retardation using array comparative genomic hybridization.
Behjati F; Firouzabadi SG; Kariminejad R; Vameghi R; Sajedi F; Shafaghati Y; Ghasemlou BE; Shojaei A; Jamali P; Bahman I; Najmabadi H
Indian J Hum Genet; 2013 Oct; 19(4):443-8. PubMed ID: 24497710
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. [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]
5. 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]
6. 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]
7. Application of array-based comparative genome hybridization in children with developmental delay or mental retardation.
Liang JS; Shimojima K; Yamamoto T
Pediatr Neonatol; 2008 Dec; 49(6):213-7. PubMed ID: 19166117
[TBL] [Abstract][Full Text] [Related]
8. Clinical utility of array CGH for the detection of chromosomal imbalances associated with mental retardation and multiple congenital anomalies.
Edelmann L; Hirschhorn K
Ann N Y Acad Sci; 2009 Jan; 1151():157-66. PubMed ID: 19154522
[TBL] [Abstract][Full Text] [Related]
9. Emerging patterns of cryptic chromosomal imbalance in patients with idiopathic mental retardation and multiple congenital anomalies: a new series of 140 patients and review of published reports.
Menten B; Maas N; Thienpont B; Buysse K; Vandesompele J; Melotte C; de Ravel T; Van Vooren S; Balikova I; Backx L; Janssens S; De Paepe A; De Moor B; Moreau Y; Marynen P; Fryns JP; Mortier G; Devriendt K; Speleman F; Vermeesch JR
J Med Genet; 2006 Aug; 43(8):625-33. PubMed ID: 16490798
[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. Clinical and molecular-cytogenetic studies of cryptic chromosome aberrations in individuals with idiopathic mental retardation and multiple congenital malformations.
Stoeva RE; Grozdanova LI; Vermeesch JR; Kirchhoff M; Fryns JP; Ivanov IS; Patcheva IH; Dimitrov BI; Krastev TB; Linev AJ; Stefanova MT
Folia Med (Plovdiv); 2008; 50(4):55-62. PubMed ID: 19209531
[TBL] [Abstract][Full Text] [Related]
12. Diagnostic utility of array-based comparative genomic hybridization in a clinical setting.
Baris HN; Tan WH; Kimonis VE; Irons MB
Am J Med Genet A; 2007 Nov; 143A(21):2523-33. PubMed ID: 17910064
[TBL] [Abstract][Full Text] [Related]
13. Clinical utility of array comparative genomic hybridisation for prenatal diagnosis: a cohort study of 3171 pregnancies.
Lee CN; Lin SY; Lin CH; Shih JC; Lin TH; Su YN
BJOG; 2012 Apr; 119(5):614-25. PubMed ID: 22313859
[TBL] [Abstract][Full Text] [Related]
14. Molecular karyotyping by array CGH in a Russian cohort of children with intellectual disability, autism, epilepsy and congenital anomalies.
Iourov IY; Vorsanova SG; Kurinnaia OS; Zelenova MA; Silvanovich AP; Yurov YB
Mol Cytogenet; 2012 Dec; 5(1):46. PubMed ID: 23272938
[TBL] [Abstract][Full Text] [Related]
15. Elucidation of a cryptic interstitial 7q31.3 deletion in a patient with a language disorder and mild mental retardation by array-CGH.
Tyson C; McGillivray B; Chijiwa C; Rajcan-Separovic E
Am J Med Genet A; 2004 Sep; 129A(3):254-60. PubMed ID: 15326624
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Defining the limits of detection for chromosome rearrangements in the preimplantation embryo using next generation sequencing.
Cuman C; Beyer CE; Brodie D; Fullston T; Lin JI; Willats E; Zander-Fox D; Mullen J
Hum Reprod; 2018 Aug; 33(8):1566-1576. PubMed ID: 30007310
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. Genetic Diagnosis of Chromosomal Congenital Anomalies in Albanian Pediatric Patients by Array CGH.
Babameto-Laku A; Roko D; Vyshka G
Open Access Maced J Med Sci; 2017 Aug; 5(5):587-591. PubMed ID: 28932296
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]