179 related articles for article (PubMed ID: 34604135)
1. Chromosomal Microarray in Children With Developmental Delay: The Experience of a Tertiary Center in Korea.
Yang EH; Shin YB; Choi SH; Yoo HW; Kim HY; Kwak MJ; Park KH; Bae MH; Kong JH; Lee YJ; Nam SO; Kim YM
Front Pediatr; 2021; 9():690493. PubMed ID: 34604135
[No Abstract] [Full Text] [Related]
2. 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]
3. 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]
4. Chromosomal Microarray Testing in 42 Korean Patients with Unexplained Developmental Delay, Intellectual Disability, Autism Spectrum Disorders, and Multiple Congenital Anomalies.
Lee SH; Song WJ
Genomics Inform; 2017 Sep; 15(3):82-86. PubMed ID: 29020723
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. A cohort study of neurodevelopmental disorders and/or congenital anomalies using high resolution chromosomal microarrays in southern Brazil highlighting the significance of ASD.
Chaves TF; Ocampos M; Barbato IT; de Camargo Pinto LL; de Luca GR; Barbato Filho JH; Bernardi P; Costa Netto Muniz Y; Francesca Maris A
Sci Rep; 2024 Feb; 14(1):3762. PubMed ID: 38355898
[TBL] [Abstract][Full Text] [Related]
7. Chromosomal Microarray Analysis as a First-Tier Clinical Diagnostic Test in Patients With Developmental Delay/Intellectual Disability, Autism Spectrum Disorders, and Multiple Congenital Anomalies: A Prospective Multicenter Study in Korea.
Jang W; Kim Y; Han E; Park J; Chae H; Kwon A; Choi H; Kim J; Son JO; Lee SJ; Hong BY; Jang DH; Han JY; Lee JH; Kim SY; Lee IG; Sung IK; Moon Y; Kim M; Park JH
Ann Lab Med; 2019 May; 39(3):299-310. PubMed ID: 30623622
[TBL] [Abstract][Full Text] [Related]
8. Utility of Chromosomal Microarray in Children with Unexplained Developmental Delay/Intellectual Disability.
Kamath V; Yoganathan S; Thomas MM; Gowri M; Chacko MP
Fetal Pediatr Pathol; 2022 Apr; 41(2):208-218. PubMed ID: 32701375
[No Abstract] [Full Text] [Related]
9. Chromosomal microarray analysis of 410 Han Chinese patients with autism spectrum disorder or unexplained intellectual disability and developmental delay.
Liu Y; Lv Y; Zarrei M; Dong R; Yang X; Higginbotham EJ; Li Y; Zhao D; Song F; Yang Y; Zhang H; Wang Y; Scherer SW; Gai Z
NPJ Genom Med; 2022 Jan; 7(1):1. PubMed ID: 35022430
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. Chromosomal Microarray Analysis of Consecutive Individuals with Autism Spectrum Disorders Using an Ultra-High Resolution Chromosomal Microarray Optimized for Neurodevelopmental Disorders.
Ho KS; Wassman ER; Baxter AL; Hensel CH; Martin MM; Prasad A; Twede H; Vanzo RJ; Butler MG
Int J Mol Sci; 2016 Dec; 17(12):. PubMed ID: 27941670
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. 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]
16. Chromosomal Aberrations in Pediatric Patients With Moderate/Severe Developmental Delay/Intellectual Disability With Abundant Phenotypic Heterogeneities: A Single-Center Study.
Wu D; Wu Y; Lan Y; Lan S; Zhong Z; Li D; Zheng Z; Wang H; Ma L
Pediatr Neurol; 2023 Oct; 147():72-81. PubMed ID: 37566956
[TBL] [Abstract][Full Text] [Related]
17. [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]
18. Copy Number Variations in a Cohort of 420 Individuals with Neurodevelopmental Disorders From the South of Brazil.
Chaves TF; Baretto N; Oliveira LF; Ocampos M; Barbato IT; Anselmi M; De Luca GR; Barbato Filho JH; Pinto LLC; Bernardi P; Maris AF
Sci Rep; 2019 Nov; 9(1):17776. PubMed ID: 31780800
[TBL] [Abstract][Full Text] [Related]
19. Copy number variant and runs of homozygosity detection by microarrays enabled more precise molecular diagnoses in 11,020 clinical exome cases.
Dharmadhikari AV; Ghosh R; Yuan B; Liu P; Dai H; Al Masri S; Scull J; Posey JE; Jiang AH; He W; Vetrini F; Braxton AA; Ward P; Chiang T; Qu C; Gu S; Shaw CA; Smith JL; Lalani S; Stankiewicz P; Cheung SW; Bacino CA; Patel A; Breman AM; Wang X; Meng L; Xiao R; Xia F; Muzny D; Gibbs RA; Beaudet AL; Eng CM; Lupski JR; Yang Y; Bi W
Genome Med; 2019 May; 11(1):30. PubMed ID: 31101064
[TBL] [Abstract][Full Text] [Related]
20. Chromosomal Microarray Analysis in Children with Unexplained Developmental Delay/Intellectual Disability.
Arican P; Olgac Dundar N; Ozyilmaz B; Cavusoglu D; Gencpinar P; Erdogan KM; Saka Guvenc M
J Pediatr Genet; 2019 Mar; 8(1):1-9. PubMed ID: 30775046
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
