217 related articles for article (PubMed ID: 34661940)
1. Diagnostic yield of microarrays in individuals with non-syndromic developmental delay and intellectual disability.
Oğuz S; Arslan UE; Kiper PÖŞ; Alikaşifoğlu M; Boduroğlu K; Utine GE
J Intellect Disabil Res; 2021 Dec; 65(12):1033-1048. PubMed ID: 34661940
[TBL] [Abstract][Full Text] [Related]
2. Application of chromosome microarray analysis in patients with unexplained developmental delay/intellectual disability in South China.
Wang R; Lei T; Fu F; Li R; Jing X; Yang X; Liu J; Li D; Liao C
Pediatr Neonatol; 2019 Feb; 60(1):35-42. PubMed ID: 29631977
[TBL] [Abstract][Full Text] [Related]
3. Application of chromosomal microarrays in the evaluation of intellectual disability/global developmental delay patients - A study from a tertiary care genetic centre in India.
Sharma P; Gupta N; Chowdhury MR; Sapra S; Ghosh M; Gulati S; Kabra M
Gene; 2016 Sep; 590(1):109-19. PubMed ID: 27291820
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. Phenotypic Analysis of Korean Patients with Abnormal Chromosomal Microarray in Patients with Unexplained Developmental Delay/Intellectual Disability.
Kim HJ; Park CI; Lim JW; Lee GM; Cho E; Kim HJ
Yonsei Med J; 2018 May; 59(3):431-437. PubMed ID: 29611406
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. Chromosomal Aberrations in Pediatric Patients with Developmental Delay/Intellectual Disability: A Single-Center Clinical Investigation.
Hu T; Zhang Z; Wang J; Li Q; Zhu H; Lai Y; Wang H; Liu S
Biomed Res Int; 2019; 2019():9352581. PubMed ID: 31781653
[TBL] [Abstract][Full Text] [Related]
10. Single nucleotide polymorphism array analysis of 102 patients with developmental delay and/or intellectual disability from Fujian, China.
Liang B; Wang Y; Lin N; Huang H; Chen L; Chen M; Yu D; Chen X; He D; Xu L
Clin Chim Acta; 2020 Nov; 510():638-643. PubMed ID: 32858057
[TBL] [Abstract][Full Text] [Related]
11. Comparing saliva and blood for the detection of mosaic genomic abnormalities that cause syndromic intellectual disability.
Francis DI; Stark Z; Scheffer IE; Tan TY; Murali K; Gallacher L; Amor DJ; Goel H; Downie L; Stutterd CA; Krzesinski EI; Vasudevan A; Oertel R; Petrovic V; Boys A; Wei V; Burgess T; Dun K; Oliver KL; Baxter A; Hackett A; Ayres S; Lunke S; Kalitsis P; Wall M
Eur J Hum Genet; 2023 May; 31(5):521-525. PubMed ID: 36446895
[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. 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]
14. [Value of copy number variation analysis and chromosomal karyotyping for the diagnosis of children with intellectual disability/developmental delay].
Lin M; Xue H; Wang Y; Huang H; Fu M; Guo N; Xu L
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 Mar; 38(3):228-231. PubMed ID: 33751530
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. Diagnostic yield of the chromosomal microarray analysis in turkish patients with unexplained development delay/ıntellectual disability(ID), autism spectrum disorders and/or multiple congenital anomalies and new clinical findings.
Akkus N; Cubuk PO
Mol Biol Rep; 2024 Apr; 51(1):577. PubMed ID: 38664339
[TBL] [Abstract][Full Text] [Related]
18. Chromosomal microarray analysis in developmental delay and intellectual disability with comorbid conditions.
Fan Y; Wu Y; Wang L; Wang Y; Gong Z; Qiu W; Wang J; Zhang H; Ji X; Ye J; Han L; Jin X; Shen Y; Li F; Xiao B; Liang L; Zhang X; Liu X; Gu X; Yu Y
BMC Med Genomics; 2018 May; 11(1):49. PubMed ID: 29793483
[TBL] [Abstract][Full Text] [Related]
19. Phenotype comparison among individuals with developmental delay/intellectual disability with or without genomic imbalances.
de Souza LC; Dos Santos AP; Sgardioli IC; Viguetti-Campos NL; Marques Prota JR; de Oliveira-Sobrinho RP; Vieira TP; Gil-da-Silva-Lopes VL
J Intellect Disabil Res; 2019 Nov; 63(11):1379-1389. PubMed ID: 30900361
[TBL] [Abstract][Full Text] [Related]
20. Chromosomal microarray analysis of Bulgarian patients with epilepsy and intellectual disability.
Peycheva V; Kamenarova K; Ivanova N; Stamatov D; Avdjieva-Tzavella D; Alexandrova I; Zhelyazkova S; Pacheva I; Dimova P; Ivanov I; Litvinenko I; Bozhinova V; Tournev I; Simeonov E; Mitev V; Jordanova A; Kaneva R
Gene; 2018 Aug; 667():45-55. PubMed ID: 29753047
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]