237 related articles for article (PubMed ID: 19917086)
1. Detection of pathogenic copy number variants in children with idiopathic intellectual disability using 500 K SNP array genomic hybridization.
Friedman J; Adam S; Arbour L; Armstrong L; Baross A; Birch P; Boerkoel C; Chan S; Chai D; Delaney AD; Flibotte S; Gibson WT; Langlois S; Lemyre E; Li HI; MacLeod P; Mathers J; Michaud JL; McGillivray BC; Patel MS; Qian H; Rouleau GA; Van Allen MI; Yong SL; Zahir FR; Eydoux P; Marra MA
BMC Genomics; 2009 Nov; 10():526. PubMed ID: 19917086
[TBL] [Abstract][Full Text] [Related]
2. Comparison of genome-wide array genomic hybridization platforms for the detection of copy number variants in idiopathic mental retardation.
Tucker T; Montpetit A; Chai D; Chan S; Chénier S; Coe BP; Delaney A; Eydoux P; Lam WL; Langlois S; Lemyre E; Marra M; Qian H; Rouleau GA; Vincent D; Michaud JL; Friedman JM
BMC Med Genomics; 2011 Mar; 4():25. PubMed ID: 21439053
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. High-resolution SNP arrays in mental retardation diagnostics: how much do we gain?
Bernardini L; Alesi V; Loddo S; Novelli A; Bottillo I; Battaglia A; Digilio MC; Zampino G; Ertel A; Fortina P; Surrey S; Dallapiccola B
Eur J Hum Genet; 2010 Feb; 18(2):178-85. PubMed ID: 19809473
[TBL] [Abstract][Full Text] [Related]
5. Single exon-resolution targeted chromosomal microarray analysis of known and candidate intellectual disability genes.
Tucker T; Zahir FR; Griffith M; Delaney A; Chai D; Tsang E; Lemyre E; Dobrzeniecka S; Marra M; Eydoux P; Langlois S; Hamdan FF; Michaud JL; Friedman JM
Eur J Hum Genet; 2014 Jun; 22(6):792-800. PubMed ID: 24253858
[TBL] [Abstract][Full Text] [Related]
6. Oligonucleotide microarray analysis of genomic imbalance in children with mental retardation.
Friedman JM; Baross A; Delaney AD; Ally A; Arbour L; Armstrong L; Asano J; Bailey DK; Barber S; Birch P; Brown-John M; Cao M; Chan S; Charest DL; Farnoud N; Fernandes N; Flibotte S; Go A; Gibson WT; Holt RA; Jones SJ; Kennedy GC; Krzywinski M; Langlois S; Li HI; McGillivray BC; Nayar T; Pugh TJ; Rajcan-Separovic E; Schein JE; Schnerch A; Siddiqui A; Van Allen MI; Wilson G; Yong SL; Zahir F; Eydoux P; Marra MA
Am J Hum Genet; 2006 Sep; 79(3):500-13. PubMed ID: 16909388
[TBL] [Abstract][Full Text] [Related]
7. Application of array comparative genomic hybridization in 256 patients with developmental delay or intellectual disability.
Bartnik M; Nowakowska B; Derwińska K; Wiśniowiecka-Kowalnik B; Kędzior M; Bernaciak J; Ziemkiewicz K; Gambin T; Sykulski M; Bezniakow N; Korniszewski L; Kutkowska-Kaźmierczak A; Klapecki J; Szczałuba K; Shaw CA; Mazurczak T; Gambin A; Obersztyn E; Bocian E; Stankiewicz P
J Appl Genet; 2014 Feb; 55(1):125-44. PubMed ID: 24297458
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. Pathogenic copy number variants and SCN1A mutations in patients with intellectual disability and childhood-onset epilepsy.
Fry AE; Rees E; Thompson R; Mantripragada K; Blake P; Jones G; Morgan S; Jose S; Mugalaasi H; Archer H; McCann E; Clarke A; Taylor C; Davies S; Gibbon F; Te Water Naude J; Hartley L; Thomas G; White C; Natarajan J; Thomas RH; Drew C; Chung SK; Rees MI; Holmans P; Owen MJ; Kirov G; Pilz DT; Kerr MP
BMC Med Genet; 2016 Apr; 17(1):34. PubMed ID: 27113213
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Copy number variants analysis in a cohort of isolated and syndromic developmental delay/intellectual disability reveals novel genomic disorders, position effects and candidate disease genes.
Di Gregorio E; Riberi E; Belligni EF; Biamino E; Spielmann M; Ala U; Calcia A; Bagnasco I; Carli D; Gai G; Giordano M; Guala A; Keller R; Mandrile G; Arduino C; Maffè A; Naretto VG; Sirchia F; Sorasio L; Ungari S; Zonta A; Zacchetti G; Talarico F; Pappi P; Cavalieri S; Giorgio E; Mancini C; Ferrero M; Brussino A; Savin E; Gandione M; Pelle A; Giachino DF; De Marchi M; Restagno G; Provero P; Cirillo Silengo M; Grosso E; Buxbaum JD; Pasini B; De Rubeis S; Brusco A; Ferrero GB
Clin Genet; 2017 Oct; 92(4):415-422. PubMed ID: 28295210
[TBL] [Abstract][Full Text] [Related]
13. Array-based comparative genomic hybridization in 190 Korean patients with developmental delay and/or intellectual disability: a single tertiary care university center study.
Lee CG; Park SJ; Yun JN; Ko JM; Kim HJ; Yim SY; Sohn YB
Yonsei Med J; 2013 Nov; 54(6):1463-70. PubMed ID: 24142652
[TBL] [Abstract][Full Text] [Related]
14. SNP arrays: comparing diagnostic yields for four platforms in children with developmental delay.
D'Amours G; Langlois M; Mathonnet G; Fetni R; Nizard S; Srour M; Tihy F; Phillips MS; Michaud JL; Lemyre E
BMC Med Genomics; 2014 Dec; 7():70. PubMed ID: 25539807
[TBL] [Abstract][Full Text] [Related]
15. Array CGH analysis of a cohort of Russian patients with intellectual disability.
Kashevarova AA; Nazarenko LP; Skryabin NA; Salyukova OA; Chechetkina NN; Tolmacheva EN; Sazhenova EA; Magini P; Graziano C; Romeo G; Kučinskas V; Lebedev IN
Gene; 2014 Feb; 536(1):145-50. PubMed ID: 24291026
[TBL] [Abstract][Full Text] [Related]
16. New insights in the interpretation of array-CGH: autism spectrum disorder and positive family history for intellectual disability predict the detection of pathogenic variants.
Cappuccio G; Vitiello F; Casertano A; Fontana P; Genesio R; Bruzzese D; Ginocchio VM; Mormile A; Nitsch L; Andria G; Melis D
Ital J Pediatr; 2016 Apr; 42():39. PubMed ID: 27072107
[TBL] [Abstract][Full Text] [Related]
17. [Application of single nucleotide polymorphism-microarray and target gene sequencing in the study of genetic etiology of children with unexplained intellectual disability or developmental delay].
Gao ZJ; Jiang Q; Cheng DZ; Yan XX; Chen Q; Xu KM
Zhonghua Er Ke Za Zhi; 2016 Oct; 54(10):740-745. PubMed ID: 27784475
[No Abstract] [Full Text] [Related]
18. Recurrent benign copy number variants & issues in interpretation of variants of unknown significance identified by cytogenetic microarray in Indian patients with intellectual disability.
Boggula VR; Agarwal M; Kumar R; Awasthi S; Phadke SR
Indian J Med Res; 2015 Dec; 142(6):699-712. PubMed ID: 26831419
[TBL] [Abstract][Full Text] [Related]
19. Oligonucleotide arrays for high-resolution analysis of copy number alteration in mental retardation/multiple congenital anomalies.
Shaikh TH
Genet Med; 2007 Sep; 9(9):617-25. PubMed ID: 17873650
[TBL] [Abstract][Full Text] [Related]
20. Genomic study via chromosomal microarray analysis in a group of Romanian patients with obesity and developmental disability/intellectual disability.
Micleaa D; Al-Khzouza C; Osan S; Bucerzan S; Cret V; Popp RA; Puiu M; Chirita-Emandi A; Zimbru C; Ghervan C
J Pediatr Endocrinol Metab; 2019 Jul; 32(7):667-674. PubMed ID: 31150357
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
