296 related articles for article (PubMed ID: 31004418)
1. 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]
2. [Application of single nucleotide polymorphism array in prenatal diagnosis for fetuses with abnormal ultrasound findings].
Guo YL; Wang L; Xue SW; Qu SZ; Yang J; Xu H; Bai ZX; Liu N; Kong XD
Zhonghua Fu Chan Ke Za Zhi; 2018 Jul; 53(7):464-470. PubMed ID: 30078256
[No Abstract] [Full Text] [Related]
3. 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]
4. [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]
5. Prenatal chromosomal microarray testing of fetuses with ultrasound structural anomalies: A prospective cohort study of over 1000 consecutive cases.
Chong HP; Hamilton S; Mone F; Cheung KW; Togneri FS; Morris RK; Quinlan-Jones E; Williams D; Allen S; McMullan DJ; Kilby MD
Prenat Diagn; 2019 Nov; 39(12):1064-1069. PubMed ID: 31393021
[TBL] [Abstract][Full Text] [Related]
6. Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study.
Lord J; McMullan DJ; Eberhardt RY; Rinck G; Hamilton SJ; Quinlan-Jones E; Prigmore E; Keelagher R; Best SK; Carey GK; Mellis R; Robart S; Berry IR; Chandler KE; Cilliers D; Cresswell L; Edwards SL; Gardiner C; Henderson A; Holden ST; Homfray T; Lester T; Lewis RA; Newbury-Ecob R; Prescott K; Quarrell OW; Ramsden SC; Roberts E; Tapon D; Tooley MJ; Vasudevan PC; Weber AP; Wellesley DG; Westwood P; White H; Parker M; Williams D; Jenkins L; Scott RH; Kilby MD; Chitty LS; Hurles ME; Maher ER;
Lancet; 2019 Feb; 393(10173):747-757. PubMed ID: 30712880
[TBL] [Abstract][Full Text] [Related]
7. Chromosomal abnormalities detected by karyotyping and microarray analysis in twins with structural anomalies.
Li L; He Z; Huang X; Lin S; Wu J; Huang L; Wan Y; Fang Q
Ultrasound Obstet Gynecol; 2020 Apr; 55(4):502-509. PubMed ID: 30977228
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Clinical utility of array comparative genomic hybridisation in prenatal setting.
Lovrecic L; Remec ZI; Volk M; Rudolf G; Writzl K; Peterlin B
BMC Med Genet; 2016 Nov; 17(1):81. PubMed ID: 27846804
[TBL] [Abstract][Full Text] [Related]
10. Chromosome copy number variants in fetuses with syndromic malformations.
Wang H; Chau MHK; Cao Y; Kwok KY; Choy KW
Birth Defects Res; 2017 Jun; 109(10):725-733. PubMed ID: 28568742
[TBL] [Abstract][Full Text] [Related]
11. Fetal congenital heart disease: Associated anomalies, identification of genetic anomalies by single-nucleotide polymorphism array analysis, and postnatal outcome.
Cai M; Huang H; Su L; Lin N; Wu X; Xie X; An G; Li Y; Lin Y; Xu L
Medicine (Baltimore); 2018 Dec; 97(50):e13617. PubMed ID: 30558042
[TBL] [Abstract][Full Text] [Related]
12. Identification of submicroscopic chromosomal aberrations in fetuses with increased nuchal translucency and apparently normal karyotype.
Leung TY; Vogel I; Lau TK; Chong W; Hyett JA; Petersen OB; Choy KW
Ultrasound Obstet Gynecol; 2011 Sep; 38(3):314-9. PubMed ID: 21400624
[TBL] [Abstract][Full Text] [Related]
13. Prenatal detection of chromosomal abnormalities and copy number variants in fetuses with congenital gastrointestinal obstruction.
Meng X; Jiang L
BMC Pregnancy Childbirth; 2022 Jan; 22(1):50. PubMed ID: 35045821
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. Detection of copy number disorders associated with congenital anomalies of the kidney and urinary tract in fetuses via single nucleotide polymorphism arrays.
Cai M; Lin N; Su L; Wu X; Xie X; Li Y; Chen X; Dai Y; Lin Y; Huang H; Xu L
J Clin Lab Anal; 2020 Jan; 34(1):e23025. PubMed ID: 31506986
[TBL] [Abstract][Full Text] [Related]
17. Prenatal diagnosis of chromosomal aberrations in fetuses with conotruncal heart defects by genome-wide high-resolution SNP array.
Lin M; Zheng J; Peng R; Du L; Zheng Q; Lei T; Xie H
J Matern Fetal Neonatal Med; 2020 Apr; 33(7):1211-1217. PubMed ID: 30149741
[No Abstract] [Full Text] [Related]
18. Copy number variations in ultrasonically abnormal late pregnancy fetuses with normal karyotypes.
Cai M; Lin N; Su L; Wu X; Xie X; Li Y; Lin Y; Xu L; Huang H
Sci Rep; 2020 Sep; 10(1):15094. PubMed ID: 32934329
[TBL] [Abstract][Full Text] [Related]
19. Prenatal detection of chromosomal abnormalities and copy number variants in fetuses with ventriculomegaly.
Chang Q; Yang Y; Peng Y; Liu S; Li L; Deng X; Yang M; Lan Y
Eur J Paediatr Neurol; 2020 Mar; 25():106-112. PubMed ID: 32014392
[TBL] [Abstract][Full Text] [Related]
20. Array-based molecular karyotyping in fetal brain malformations: Identification of novel candidate genes and chromosomal regions.
Krutzke SK; Engels H; Hofmann A; Schumann MM; Cremer K; Zink AM; Hilger A; Ludwig M; Gembruch U; Reutter H; Merz WM
Birth Defects Res A Clin Mol Teratol; 2016 Jan; 106(1):16-26. PubMed ID: 26680650
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
