436 related articles for article (PubMed ID: 22025351)
1. Prenatal genetic diagnosis using microarray analysis in fetuses with congenital heart defects.
Schmid M; Stary S; Blaicher W; Gollinger M; Husslein P; Streubel B
Prenat Diagn; 2012 Apr; 32(4):376-82. PubMed ID: 22025351
[TBL] [Abstract][Full Text] [Related]
2. Detection of submicroscopic chromosomal aberrations by array-based comparative genomic hybridization in fetuses with congenital heart disease.
Yan Y; Wu Q; Zhang L; Wang X; Dan S; Deng D; Sun L; Yao L; Ma Y; Wang L
Ultrasound Obstet Gynecol; 2014 Apr; 43(4):404-12. PubMed ID: 24323407
[TBL] [Abstract][Full Text] [Related]
3. Prenatal chromosomal microarray analysis in fetuses with congenital heart disease: a prospective cohort study.
Wang Y; Cao L; Liang D; Meng L; Wu Y; Qiao F; Ji X; Luo C; Zhang J; Xu T; Yu B; Wang L; Wang T; Pan Q; Ma D; Hu P; Xu Z
Am J Obstet Gynecol; 2018 Feb; 218(2):244.e1-244.e17. PubMed ID: 29128521
[TBL] [Abstract][Full Text] [Related]
4. Prenatal diagnosis and molecular cytogenetic characterization of chromosome 22q11.2 deletion syndrome associated with congenital heart defects.
Kuo YL; Chen CP; Wang LK; Ko TM; Chang TY; Chern SR; Wu PS; Chen YT; Chang SY
Taiwan J Obstet Gynecol; 2014 Jun; 53(2):248-51. PubMed ID: 25017279
[TBL] [Abstract][Full Text] [Related]
5. Prospective chromosome analysis of 3429 amniocentesis samples in China using copy number variation sequencing.
Wang J; Chen L; Zhou C; Wang L; Xie H; Xiao Y; Zhu H; Hu T; Zhang Z; Zhu Q; Liu Z; Liu S; Wang H; Xu M; Ren Z; Yu F; Cram DS; Liu H
Am J Obstet Gynecol; 2018 Sep; 219(3):287.e1-287.e18. PubMed ID: 29852155
[TBL] [Abstract][Full Text] [Related]
6. Validation of a Chromosomal Microarray for Prenatal Diagnosis Using a Prospective Cohort of Pregnancies with Increased Risk for Chromosome Abnormalities.
Wright D; Carey L; Battersby S; Nguyen T; Clarke M; Nash B; Gulesserian E; Cross J; Darmanian A
Genet Test Mol Biomarkers; 2016 Dec; 20(12):791-798. PubMed ID: 27690282
[TBL] [Abstract][Full Text] [Related]
7. Identification of copy number variations associated with congenital heart disease by chromosomal microarray analysis and next-generation sequencing.
Zhu X; Li J; Ru T; Wang Y; Xu Y; Yang Y; Wu X; Cram DS; Hu Y
Prenat Diagn; 2016 Apr; 36(4):321-7. PubMed ID: 26833920
[TBL] [Abstract][Full Text] [Related]
8. Prenatal diagnosis of a trisomy 7 mosaic case: CMA, CNV-seq, karyotyping, interphase FISH, and MS-MLPA, which technique to choose?
Cong X; Zhang T; Li Z; Luo X; Hu L; Liu W
BMC Pregnancy Childbirth; 2024 May; 24(1):338. PubMed ID: 38702634
[TBL] [Abstract][Full Text] [Related]
9. [Combined G-banded karyotyping and multiplex ligation-dependent probe amplification for the detection of chromosomal abnormalities in fetuses with congenital heart defects].
Liu Y; Xie J; Geng Q; Xu Z; Wu W; Luo F; Li S; Wang Q; Chen W; Tan H; Zhang H
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Feb; 34(1):1-5. PubMed ID: 28186583
[TBL] [Abstract][Full Text] [Related]
10. Prenatal diagnosis of chromosomal abnormalities in fetuses with abnormal cardiac ultrasound findings: evaluation of chromosomal microarray-based analysis.
Mademont-Soler I; Morales C; Soler A; Martínez-Crespo JM; Shen Y; Margarit E; Clusellas N; Obón M; Wu BL; Sánchez A
Ultrasound Obstet Gynecol; 2013 Apr; 41(4):375-82. PubMed ID: 23233332
[TBL] [Abstract][Full Text] [Related]
11. [Application of chromosome microarray analysis for prenatal diagnosis of a fetus with partial duplication of 1p and uniparental disomy of chromosome 6].
Zhu R; Zhu X; Wang Y; Li J; Ru T; Yang Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Dec; 32(6):819-22. PubMed ID: 26663056
[TBL] [Abstract][Full Text] [Related]
12. Detection of Chromosomal Aberrations in Clinical Practice: From Karyotype to Genome Sequence.
Martin CL; Warburton D
Annu Rev Genomics Hum Genet; 2015; 16():309-26. PubMed ID: 26077817
[TBL] [Abstract][Full Text] [Related]
13. [Karyotype analysis of amniotic fluid cells and comparison of chromosomal abnormality rate during second trimester].
Zhang YP; Wu JP; Li XT; Lei CX; Xu JZ; Yin M
Zhonghua Fu Chan Ke Za Zhi; 2011 Sep; 46(9):644-8. PubMed ID: 22176986
[TBL] [Abstract][Full Text] [Related]
14. [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]
15. [Improved identification for 5p deletion syndrome and partial trisomy 11q presented in a fetus by SNP array].
Shi S; Pan G; Yang Y; Yan R; Li W
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Apr; 33(2):195-9. PubMed ID: 27060314
[TBL] [Abstract][Full Text] [Related]
16. Clinical application of SNP array analysis in fetuses with ventricular septal defects and normal karyotypes.
Fu F; Deng Q; Lei TY; Li R; Jing XY; Yang X; Liao C
Arch Gynecol Obstet; 2017 Nov; 296(5):929-940. PubMed ID: 28905115
[TBL] [Abstract][Full Text] [Related]
17. [Application of whole-genome and high-resolution chromosome microarray analysis for the investigation of fetuses with ultrasound abnormalities].
Zhang Y; Fu F; Li R; Xie G; Han J; Pan M; Zhen L; Yang X; Li D; Liao C
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Apr; 32(2):169-74. PubMed ID: 25863078
[TBL] [Abstract][Full Text] [Related]
18. [Detection of mosaic trisomy 9 missed by conventional cytogenetics using SNP-array and fluorescence in situ hybridization].
Luo Y; Chen S; Li H; Pan L; Shen M; Jin F; Xu C
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Aug; 31(4):469-71. PubMed ID: 25119912
[TBL] [Abstract][Full Text] [Related]
19. Association of structural and numerical anomalies of chromosome 22 in a patient with syndromic intellectual disability.
Naoufal R; Legendre M; Couet D; Gilbert-Dussardier B; Kitzis A; Bilan F; Harbuz R
Eur J Med Genet; 2016 Sep; 59(9):483-7. PubMed ID: 27452446
[TBL] [Abstract][Full Text] [Related]
20. Prenatal chromosomal microarray analysis in a diagnostic laboratory; experience with >1000 cases and review of the literature.
Breman A; Pursley AN; Hixson P; Bi W; Ward P; Bacino CA; Shaw C; Lupski JR; Beaudet A; Patel A; Cheung SW; Van den Veyver I
Prenat Diagn; 2012 Apr; 32(4):351-61. PubMed ID: 22467166
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
