155 related articles for article (PubMed ID: 24692221)
1. Re: Detection of submicroscopic chromosomal aberrations by array-based comparative genomic hybridization in fetuses with congenital heart disease. Y. Yan, Q. Wu, L. Zhang, X. Wang, S. Dan, D. Deng, L. Sun, L. Yao, Y. Ma and L. Wang. Ultrasound Obstet Gynecol 2014; 43: 404-412.
de Wit MC
Ultrasound Obstet Gynecol; 2014 Apr; 43(4):363. PubMed ID: 24692221
[No 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 Diagnosis by Array Comparative Genomic Hybridization in Fetuses with Cardiac Abnormalities.
Kowalczyk K; Bartnik-Głaska M; Smyk M; Plaskota I; Bernaciak J; Kędzior M; Wiśniowiecka-Kowalnik B; Jakubów-Durska K; Braun-Walicka N; Barczyk A; Geremek M; Castañeda J; Kutkowska-Kaźmierczak A; Własienko P; Dębska M; Kucińska-Chahwan A; Roszkowski T; Kozłowski S; Mikulska B; Issat T; Obersztyn E; Nowakowska BA
Genes (Basel); 2021 Dec; 12(12):. PubMed ID: 34946970
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. [Application of array comparative genomic hybridization analysis for fetuses with growth anomalies].
Wang L; Wang X; Cai N; He B; Wu Q; Li W; Zhang L; Ma X; Qiang R
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Oct; 34(5):691-694. PubMed ID: 28981935
[TBL] [Abstract][Full Text] [Related]
6. Phenotype to genotype characterization by array-comparative genomic hydridization (a-CGH) in case of fetal malformations: A systematic review.
Tonni G; Palmisano M; Perez Zamarian AC; Rabachini Caetano AC; Santana EFM; Peixoto AB; Armbruster-Moraes E; Ruano R; Araujo Júnior E
Taiwan J Obstet Gynecol; 2019 Jan; 58(1):15-28. PubMed ID: 30638470
[TBL] [Abstract][Full Text] [Related]
7. Re: prenatal diagnosis using combined quantitative fluorescent polymerase chain reaction and array comparative genomic hybridization analysis as a first-line test: results from over 1000 consecutive cases. F. Scott, K. Murphy, L. Carey, W. Greville, N. Mansfield, P. Barahona, R. Robertson and A. McLennan. Ultrasound Obstet Gynecol 2013; 41: 500-507.
Mansour S
Ultrasound Obstet Gynecol; 2013 May; 41(5):489. PubMed ID: 23610035
[No Abstract] [Full Text] [Related]
8. Cardiovascular Anomalies among 1005 Fetuses Referred to Invasive Prenatal Testing-A Comprehensive Cohort Study of Associated Chromosomal Aberrations.
Wójtowicz A; Madetko-Talowska A; Wójtowicz W; Szewczyk K; Huras H; Bik-Multanowski M
Int J Environ Res Public Health; 2022 Aug; 19(16):. PubMed ID: 36011653
[TBL] [Abstract][Full Text] [Related]
9. The frequency of CNVs in a cohort population of consecutive fetuses with congenital anomalies after the termination of pregnancy.
Rudolf G; Lovrečić L; Tul N; Teran N; Peterlin B
Mol Genet Genomic Med; 2019 Jun; 7(6):e658. PubMed ID: 31004418
[TBL] [Abstract][Full Text] [Related]
10. [Detection of cryptic copy number variations in a fetus with congenital heart disease by array-based comparative genomic hybridization].
HU P; WANG Y; JI XQ; LIN Y; Li L; ZHOU XY; CHEN J; MA DY; CAO L; Xu Z
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Apr; 28(2):133-6. PubMed ID: 21462121
[TBL] [Abstract][Full Text] [Related]
11. Clinical utility of array comparative genomic hybridisation for prenatal diagnosis: a cohort study of 3171 pregnancies.
Lee CN; Lin SY; Lin CH; Shih JC; Lin TH; Su YN
BJOG; 2012 Apr; 119(5):614-25. PubMed ID: 22313859
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Array comparative genomic hybridization and fetal congenital heart defects: a systematic review and meta-analysis.
Jansen FA; Blumenfeld YJ; Fisher A; Cobben JM; Odibo AO; Borrell A; Haak MC
Ultrasound Obstet Gynecol; 2015 Jan; 45(1):27-35. PubMed ID: 25319878
[TBL] [Abstract][Full Text] [Related]
14. Identification of De Novo and Rare Inherited Copy Number Variants in Children with Syndromic Congenital Heart Defects.
Hussein IR; Bader RS; Chaudhary AG; Bassiouni R; Alquaiti M; Ashgan F; Schulten HJ; Al Qahtani MH
Pediatr Cardiol; 2018 Jun; 39(5):924-940. PubMed ID: 29541814
[TBL] [Abstract][Full Text] [Related]
15. [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]
16. Clinical application of chromosomal microarray analysis for the prenatal diagnosis of chromosomal abnormalities and copy number variations in fetuses with congenital heart disease.
Xia Y; Yang Y; Huang S; Wu Y; Li P; Zhuang J
Prenat Diagn; 2018 May; 38(6):406-413. PubMed ID: 29573438
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Copy number imbalances detected with a BAC-based array comparative genomic hybridization platform in congenital diaphragmatic hernia fetuses.
Machado IN; Heinrich JK; Barini R; Peralta CF
Genet Mol Res; 2011 Feb; 10(1):261-7. PubMed ID: 21341218
[TBL] [Abstract][Full Text] [Related]
19. Re: Diagnosis of fetal submicroscopic chromosomal abnormalities in failed array CGH samples: copy number by sequencing as an alternative to microarrays for invasive fetal testing. K. Cohen, A. Tzika, H. Wood, S. Berri, P. Roberts, G. Mason and E. Sheridan. Ultrasound Obstet Gynecol 2015; 45: 394-401.
McMullan DJ
Ultrasound Obstet Gynecol; 2015 Apr; 45(4):373-4. PubMed ID: 25833368
[No Abstract] [Full Text] [Related]
20. Submicroscopic chromosomal abnormalities in fetuses with increased nuchal translucency and normal karyotype.
Yang X; Li R; Fu F; Zhang Y; Li D; Liao C
J Matern Fetal Neonatal Med; 2017 Jan; 30(2):194-198. PubMed ID: 26998667
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
