1145 related articles for article (PubMed ID: 31337399)
1. 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]
2. 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]
3. 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]
4. 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]
5. [Molecular diagnosis of children with unexplained intellectual disability/ developmental delay by array-CGH].
He XY; Chen XC; Li R; Li P; Lu AM
Zhongguo Dang Dai Er Ke Za Zhi; 2015 May; 17(5):459-63. PubMed ID: 26014695
[TBL] [Abstract][Full Text] [Related]
6. Array CGH in patients with developmental delay or intellectual disability: are there phenotypic clues to pathogenic copy number variants?
Shoukier M; Klein N; Auber B; Wickert J; Schröder J; Zoll B; Burfeind P; Bartels I; Alsat EA; Lingen M; Grzmil P; Schulze S; Keyser J; Weise D; Borchers M; Hobbiebrunken E; Röbl M; Gärtner J; Brockmann K; Zirn B
Clin Genet; 2013 Jan; 83(1):53-65. PubMed ID: 22283495
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Cognitive deficit and autism spectrum disorders: prospective diagnosis by array CGH.
Nicholl J; Waters W; Mulley JC; Suwalski S; Brown S; Hull Y; Barnett C; Haan E; Thompson EM; Liebelt J; Mcgregor L; Harbord MG; Entwistle J; Munt C; White D; Chitti A; Baulderstone D; Ketteridge D; ; Friend K; Bain SM; Yu S
Pathology; 2014 Jan; 46(1):41-5. PubMed ID: 24300712
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. 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]
12. [The diagnostic value of chromosome microarray analysis technique in the genetic causes of children with intellectual disability or global developmental delay].
Wu HR; Li L; Ma YN; Liu CL; Pei P; Zheng XF; Wang ST; Xiao Y; Bu DF; Xu YF; Pan H; Qi Y
Zhonghua Yi Xue Za Zhi; 2021 Jan; 101(3):224-228. PubMed ID: 33455150
[No Abstract] [Full Text] [Related]
13. Application of array comparative genomic hybridization in 102 patients with epilepsy and additional neurodevelopmental disorders.
Bartnik M; Szczepanik E; Derwińska K; Wiśniowiecka-Kowalnik B; Gambin T; Sykulski M; Ziemkiewicz K; Kędzior M; Gos M; Hoffman-Zacharska D; Mazurczak T; Jeziorek A; Antczak-Marach D; Rudzka-Dybała M; Mazurkiewicz H; Goszczańska-Ciuchta A; Zalewska-Miszkurka Z; Terczyńska I; Sobierajewicz M; Shaw CA; Gambin A; Mierzewska H; Mazurczak T; Obersztyn E; Bocian E; Stankiewicz P
Am J Med Genet B Neuropsychiatr Genet; 2012 Oct; 159B(7):760-71. PubMed ID: 22825934
[TBL] [Abstract][Full Text] [Related]
14. Chromosomal microarray in clinical diagnosis: a study of 337 patients with congenital anomalies and developmental delays or intellectual disability.
Sansović I; Ivankov AM; Bobinec A; Kero M; Barišić I
Croat Med J; 2017 Jun; 58(3):231-238. PubMed ID: 28613040
[TBL] [Abstract][Full Text] [Related]
15. Routine chromosomal microarray analysis is necessary in Korean patients with unexplained developmental delay/mental retardation/autism spectrum disorder.
Shin S; Yu N; Choi JR; Jeong S; Lee KA
Ann Lab Med; 2015 Sep; 35(5):510-8. PubMed ID: 26206688
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
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. 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]
20. 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]
[Next] [New Search]
