173 related articles for article (PubMed ID: 19490664)
21. The Diagnostic Yield of Array Comparative Genomic Hybridization Is High Regardless of Severity of Intellectual Disability/Developmental Delay in Children.
D'Arrigo S; Gavazzi F; Alfei E; Zuffardi O; Montomoli C; Corso B; Buzzi E; Sciacca FL; Bulgheroni S; Riva D; Pantaleoni C
J Child Neurol; 2016 May; 31(6):691-9. PubMed ID: 26511719
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. [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]
24. "Familial" versus "sporadic" intellectual disability: contribution of subtelomeric rearrangements.
Rafati M; Ghadirzadeh MR; Heshmati Y; Adibi H; Keihanidoust Z; Eshraghian MR; Dastan J; Hoseini A; Purhoseini M; Ghaffari SR
Mol Cytogenet; 2012 Jan; 5(1):4. PubMed ID: 22260313
[TBL] [Abstract][Full Text] [Related]
25. Chromosomal Microarray With Clinical Diagnostic Utility in Children With Developmental Delay or Intellectual Disability.
Lee JS; Hwang H; Kim SY; Kim KJ; Choi JS; Woo MJ; Choi YM; Jun JK; Lim BC; Chae JH
Ann Lab Med; 2018 Sep; 38(5):473-480. PubMed ID: 29797819
[TBL] [Abstract][Full Text] [Related]
26. Subtelomeric study of 132 patients with mental retardation reveals 9 chromosomal anomalies and contributes to the delineation of submicroscopic deletions of 1pter, 2qter, 4pter, 5qter and 9qter.
Sogaard M; Tümer Z; Hjalgrim H; Hahnemann J; Friis B; Ledaal P; Pedersen VF; Baekgaard P; Tommerup N; Cingöz S; Duno M; Brondum-Nielsen K
BMC Med Genet; 2005 May; 6():21. PubMed ID: 15904506
[TBL] [Abstract][Full Text] [Related]
27. Screening of subtelomeric rearrangements in 100 Korean Pediatric patients with unexplained mental retardation and anomalies using subtelomeric FISH (fluorescence in situ hybridization).
Park HK; Kim HJ; Kim HJ; Han SH; Kim YJ; Kim SH
J Korean Med Sci; 2008 Aug; 23(4):573-8. PubMed ID: 18756040
[TBL] [Abstract][Full Text] [Related]
28. [Chromosome subtelomeric analysis by FISH in patients with mental retardation].
Li R; Zhao ZY; Pai S
Zhejiang Da Xue Xue Bao Yi Xue Ban; 2004 Jul; 33(4):349-52. PubMed ID: 15269989
[TBL] [Abstract][Full Text] [Related]
29. Long contiguous stretches of homozygosity spanning shortly the imprinted loci are associated with intellectual disability, autism and/or epilepsy.
Iourov IY; Vorsanova SG; Korostelev SA; Zelenova MA; Yurov YB
Mol Cytogenet; 2015; 8():77. PubMed ID: 26478745
[TBL] [Abstract][Full Text] [Related]
30. Cytogenomic Evaluation of Children with Congenital Anomalies: Critical Implications for Diagnostic Testing and Genetic Counseling.
Szczałuba K; Jakubiuk-Tomaszuk A; Kędzior M; Bernaciak J; Zdrodowska J; Kurzątkowski W; Radkowski M; Demkow U
Adv Exp Med Biol; 2016; 912():11-9. PubMed ID: 26987321
[TBL] [Abstract][Full Text] [Related]
31. Multiplex ligation-dependent probe amplification workflow for the detection of submicroscopic chromosomal abnormalities in patients with developmental delay/intellectual disability.
Pohovski LM; Dumic KK; Odak L; Barisic I
Mol Cytogenet; 2013 Feb; 6(1):7. PubMed ID: 23383958
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. Comparison of two subtelomeric assays for the screening of chromosomal rearrangements: analysis of 383 patients, literature review and further recommendations.
Santa María L; Faundes V; Curotto B; Morales P; Morales K; Aliaga S; Pugin Á; Alliende MA
J Appl Genet; 2016 Feb; 57(1):63-9. PubMed ID: 26069167
[TBL] [Abstract][Full Text] [Related]
34. An unbalanced half-cryptic translocation involving the 6q subtelomeric region and 2p25.3 in a child with mental retardation: uses and limitations of fluorescence in situ hybridization.
Batanian JR; Hussain MI
Clin Genet; 1999 Apr; 55(4):265-8. PubMed ID: 10361988
[TBL] [Abstract][Full Text] [Related]
35. 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]
36. The usefulness of array comparative genomic hybridization in clinical diagnostics of intellectual disability in children.
Bartnik M; Wiśniowiecka-Kowalnik B; Nowakowska B; Smyk M; Kędzior M; Sobecka K; Kutkowska-Kaźmierczak A; Klapecki J; Szczałuba K; Castañeda J; Własienko P; Bezniakow N; Obersztyn E; Bocian E
Dev Period Med; 2014; 18(3):307-17. PubMed ID: 25182394
[TBL] [Abstract][Full Text] [Related]
37. Subtelomeric Rearrangements in Patients with Recurrent Miscarriage.
Hajlaoui A; Slimani W; Kammoun M; Sallem A; El Amri F; Chaieb A; Bibi M; Saad A; Mougou-Zerelli S
Int J Fertil Steril; 2018 Jun; 12(3):218-222. PubMed ID: 29935067
[TBL] [Abstract][Full Text] [Related]
38. Detection of genomic imbalances by array based comparative genomic hybridisation in fetuses with multiple malformations.
Le Caignec C; Boceno M; Saugier-Veber P; Jacquemont S; Joubert M; David A; Frebourg T; Rival JM
J Med Genet; 2005 Feb; 42(2):121-8. PubMed ID: 15689449
[TBL] [Abstract][Full Text] [Related]
39. 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]
40. Array-CGH analysis in patients with intellectual disability and/or congenital malformations in Brazil.
Vianna GS; Medeiros PF; Alves AF; Silva TO; Jehee FS
Genet Mol Res; 2016 Feb; 15(1):. PubMed ID: 26909975
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
