193 related articles for article (PubMed ID: 32820506)
1. [Detection of genomic copy number variations in patients with unexplained mental retardation/developmental delay by low coverage whole-genome sequencing].
Song H; Shi P; Xiao Y; Hou Y; Chen D; Kong X
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Sep; 37(9):953-957. PubMed ID: 32820506
[TBL] [Abstract][Full Text] [Related]
2. [Analysis of copy number variations in 66 children with unexplained mental retardation/developmental delay using chromosomal microarrays].
Li Y; Qiu W; Ye J; Han L; Zhang H; Gu X
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Dec; 31(6):703-7. PubMed ID: 25449071
[TBL] [Abstract][Full Text] [Related]
3. [Application of copy number variation sequencing in patients with intellectual disability/developmental delay and autistic spectrum disorder].
Lei J; Zhao G; Huang Y; Long M; Li W; Deng X; Xiu Z; Xiao Y; Zeng S; Zhang J
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Mar; 40(3):308-316. PubMed ID: 36854406
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. [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]
6. 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]
7. 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]
8. 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]
9. [Clinical phenotypes and copy number variations in children with microdeletion and microduplication syndromes: an analysis of 50 cases].
Zhang LN; Meng Z; He ZW; Li DF; Luo XY; Liang LY
Zhongguo Dang Dai Er Ke Za Zhi; 2016 Sep; 18(9):840-845. PubMed ID: 27655541
[TBL] [Abstract][Full Text] [Related]
10. Submicroscopic subtelomeric aberrations in Chinese patients with unexplained developmental delay/mental retardation.
Wu Y; Ji T; Wang J; Xiao J; Wang H; Li J; Gao Z; Yang Y; Cai B; Wang L; Zhou Z; Tian L; Wang X; Zhong N; Qin J; Wu X; Jiang Y
BMC Med Genet; 2010 May; 11():72. PubMed ID: 20459802
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. [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]
13. 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]
14. CNV analysis in Chinese children of mental retardation highlights a sex differentiation in parental contribution to de novo and inherited mutational burdens.
Wang B; Ji T; Zhou X; Wang J; Wang X; Wang J; Zhu D; Zhang X; Sham PC; Zhang X; Ma X; Jiang Y
Sci Rep; 2016 Jun; 6():25954. PubMed ID: 27257017
[TBL] [Abstract][Full Text] [Related]
15. Clinical utility of multiplex ligation-dependent probe amplification technique in identification of aetiology of unexplained mental retardation: a study in 203 Indian patients.
Boggula VR; Shukla A; Danda S; Hariharan SV; Nampoothiri S; Kumar R; Phadke SR
Indian J Med Res; 2014 Jan; 139(1):66-75. PubMed ID: 24604040
[TBL] [Abstract][Full Text] [Related]
16. [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]
17. Delineating the psychiatric and behavioral phenotype of recurrent 2q13 deletions and duplications.
Wolfe K; McQuillin A; Alesi V; Boudry Labis E; Cutajar P; Dallapiccola B; Dentici ML; Dieux-Coeslier A; Duban-Bedu B; Duelund Hjortshøj T; Goel H; Loddo S; Morrogh D; Mosca-Boidron AL; Novelli A; Olivier-Faivre L; Parker J; Parker MJ; Patch C; Pelling AL; Smol T; Tümer Z; Vanakker O; van Haeringen A; Vanlerberghe C; Strydom A; Skuse D; Bass N
Am J Med Genet B Neuropsychiatr Genet; 2018 Jun; 177(4):397-405. PubMed ID: 29603867
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. [Clinical and genetic analysis of three children patients with Kleefstra syndrome].
Zhou T; Tong G; Zhu L; Li S; Li H; Dong W
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2022 Feb; 39(2):148-151. PubMed ID: 35076909
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]