176 related articles for article (PubMed ID: 28918392)
21. Detection of fetal copy number variants by non-invasive prenatal testing for common aneuploidies.
Li R; Wan J; Zhang Y; Fu F; Ou Y; Jing X; Li J; Li D; Liao C
Ultrasound Obstet Gynecol; 2016 Jan; 47(1):53-7. PubMed ID: 26033469
[TBL] [Abstract][Full Text] [Related]
22. Detection of copy number variants and genes by chromosomal microarray in an Emirati neurodevelopmental disorders cohort.
Nassir N; Sati I; Al Shaibani S; Ahmed A; Almidani O; Akter H; Woodbury-Smith M; Tayoun AA; Uddin M; Albanna A
Neurogenetics; 2022 Apr; 23(2):137-149. PubMed ID: 35325322
[TBL] [Abstract][Full Text] [Related]
23. Impact of IQ on the diagnostic yield of chromosomal microarray in a community sample of adults with schizophrenia.
Lowther C; Merico D; Costain G; Waserman J; Boyd K; Noor A; Speevak M; Stavropoulos DJ; Wei J; Lionel AC; Marshall CR; Scherer SW; Bassett AS
Genome Med; 2017 Nov; 9(1):105. PubMed ID: 29187259
[TBL] [Abstract][Full Text] [Related]
24. 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]
25. Clinical relevance of small copy-number variants in chromosomal microarray clinical testing.
Hollenbeck D; Williams CL; Drazba K; Descartes M; Korf BR; Rutledge SL; Lose EJ; Robin NH; Carroll AJ; Mikhail FM
Genet Med; 2017 Apr; 19(4):377-385. PubMed ID: 27632688
[TBL] [Abstract][Full Text] [Related]
26. Copy number variations in multicystic dysplastic kidney: update for prenatal diagnosis and genetic counseling.
Xi Q; Zhu X; Wang Y; Ru T; Dai C; Wang Z; Li J; Hu Y
Prenat Diagn; 2016 May; 36(5):463-8. PubMed ID: 26941192
[TBL] [Abstract][Full Text] [Related]
27. [Application of chromosomal microarray analysis for fetuses with ventricular septal defects].
Deng Q; Fu F; Li R; Jing X; Lei T; Yang X; Pan M; Zhen L; Han J; Liao C
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Oct; 34(5):699-704. PubMed ID: 28981937
[TBL] [Abstract][Full Text] [Related]
28. Concordance between somatic copy number loss and down-regulated expression: A pan-cancer study of cancer predisposition genes.
Wei R; Zhao M; Zheng CH; Zhao M; Xia J
Sci Rep; 2016 Dec; 6():37358. PubMed ID: 27929028
[TBL] [Abstract][Full Text] [Related]
29. High-resolution SNP genotyping platform identified recurrent and novel CNVs in autism multiplex families.
AlAyadhi LY; Hashmi JA; Iqbal M; Albalawi AM; Samman MI; Elamin NE; Bashir S; Basit S
Neuroscience; 2016 Dec; 339():561-570. PubMed ID: 27771533
[TBL] [Abstract][Full Text] [Related]
30. Chromosome microarrays in diagnostic testing: interpreting the genomic data.
Peters GB; Pertile MD
Methods Mol Biol; 2014; 1168():117-55. PubMed ID: 24870134
[TBL] [Abstract][Full Text] [Related]
31. Identification of recurrent focal copy number variations and their putative targeted driver genes in ovarian cancer.
Zhang L; Yuan Y; Lu KH; Zhang L
BMC Bioinformatics; 2016 May; 17(1):222. PubMed ID: 27230211
[TBL] [Abstract][Full Text] [Related]
32. High resolution chromosomal microarray in undiagnosed neurological disorders.
Howell KB; Kornberg AJ; Harvey AS; Ryan MM; Mackay MT; Freeman JL; Rodriguez Casero MV; Collins KJ; Hayman M; Mohamed A; Ware TL; Clark D; Bruno DL; Burgess T; Slater H; McGillivray G; Leventer RJ
J Paediatr Child Health; 2013 Sep; 49(9):716-24. PubMed ID: 23731025
[TBL] [Abstract][Full Text] [Related]
33. 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]
34. [Prenatal diagnosis of a fetus with cleft lip and palate by using chromosomal microarray analysis].
Huang C; Song X; Zhang Q; Liu M; Mao J; Xiang J; Liu Y; Li H; Wang T
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Apr; 37(4):471-474. PubMed ID: 32219840
[TBL] [Abstract][Full Text] [Related]
35. Copy number alterations involving 59 ACMG-recommended secondary findings genes.
Yatsenko SA; Aarabi M; Hu J; Surti U; Ortiz D; Madan-Khetarpal S; Saller DN; Bellissimo D; Rajkovic A
Clin Genet; 2020 Dec; 98(6):577-588. PubMed ID: 33009833
[TBL] [Abstract][Full Text] [Related]
36. [Clinical value of genome-wide high resolution chromosomal microarray analysis in etiological study of fetuses with congenital heart defects].
Wu X; Fu F; Li R; Pan M; Han J; Zhen L; Yang X; Zhang Y; Li F; Liao C
Zhonghua Fu Chan Ke Za Zhi; 2014 Dec; 49(12):893-8. PubMed ID: 25608988
[TBL] [Abstract][Full Text] [Related]
37. Burden of potentially pathologic copy number variants is higher in children with isolated congenital heart disease and significantly impairs covariate-adjusted transplant-free survival.
Kim DS; Kim JH; Burt AA; Crosslin DR; Burnham N; Kim CE; McDonald-McGinn DM; Zackai EH; Nicolson SC; Spray TL; Stanaway IB; Nickerson DA; Heagerty PJ; Hakonarson H; Gaynor JW; Jarvik GP
J Thorac Cardiovasc Surg; 2016 Apr; 151(4):1147-51.e4. PubMed ID: 26704054
[TBL] [Abstract][Full Text] [Related]
38. Rare germline copy number deletions of likely functional importance are implicated in endometrial cancer predisposition.
Moir-Meyer GL; Pearson JF; Lose F; ; Scott RJ; McEvoy M; Attia J; Holliday EG; ; ; Pharoah PD; Dunning AM; Thompson DJ; Easton DF; Spurdle AB; Walker LC
Hum Genet; 2015 Mar; 134(3):269-78. PubMed ID: 25381466
[TBL] [Abstract][Full Text] [Related]
39. Genome-wide copy number analysis in a family with p.G533C RET mutation and medullary thyroid carcinoma identified regions potentially associated with a higher predisposition to lymph node metastasis.
Araujo AN; Moraes L; França MI; Hakonarson H; Li J; Pellegrino R; Maciel RM; Cerutti JM
J Clin Endocrinol Metab; 2014 Jun; 99(6):E1104-12. PubMed ID: 24601688
[TBL] [Abstract][Full Text] [Related]
40. Leveraging Unique Chromosomal Microarray Probes to Accurately Detect Copy Number at the Highly Homologous 15q15.3 Deafness-Infertility Syndrome Locus.
Sack LM; Mertens L; Murphy E; Hutchinson L; Giersch ABS; Mason-Suares H
Clin Chem; 2023 Jun; 69(6):583-594. PubMed ID: 37022747
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
