153 related articles for article (PubMed ID: 36343605)
1. Prenatal diagnosis study using array comparative genomic hybridization for genotype-phenotype correlation in 772 fetuses.
Costa BC; Grangeia A; Galvão J; Vaz D; Melo M; Carraca T; Ramalho C; Dória S
Ann Diagn Pathol; 2022 Dec; 61():152059. PubMed ID: 36343605
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Comparative Genomic Hybridization to Microarrays in Fetuses with High-Risk Prenatal Indications: Polish Experience with 7400 Pregnancies.
Kowalczyk K; Bartnik-Głaska M; Smyk M; Plaskota I; Bernaciak J; Kędzior M; Wiśniowiecka-Kowalnik B; Deperas M; Domaradzka J; Łuszczek A; Dutkiewicz D; Kozar A; Grad D; Niemiec M; Ziemkiewicz K; Magdziak R; Braun-Walicka N; Barczyk A; Geremek M; Castañeda J; Kutkowska-Kaźmierczak A; Własienko P; Jakubów-Durska K; Dębska M; Kucińska-Chahwan A; Kozłowski S; Mikulska B; Issat T; Roszkowski T; Nawara-Baran A; Runge A; Jakubiuk-Tomaszuk A; Kruczek A; Kostyk E; Pietras G; Limon J; Zwoliński J; Ochman K; Szajner T; Węgrzyn P; Wielgoś M; Sąsiadek M; Obersztyn E; Nowakowska BA
Genes (Basel); 2022 Apr; 13(4):. PubMed ID: 35456496
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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.
Scott F; Murphy K; Carey L; Greville W; Mansfield N; Barahona P; Robertson R; McLennan A
Ultrasound Obstet Gynecol; 2013 May; 41(5):500-7. PubMed ID: 23401365
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Application of chromosomal microarray in the evaluation of abnormal prenatal findings.
Yatsenko SA; Davis S; Hendrix NW; Surti U; Emery S; Canavan T; Speer P; Hill L; Clemens M; Rajkovic A
Clin Genet; 2013 Jul; 84(1):47-54. PubMed ID: 23020214
[TBL] [Abstract][Full Text] [Related]
8. Genomic microarray in fetuses with increased nuchal translucency and normal karyotype: a systematic review and meta-analysis.
Grande M; Jansen FA; Blumenfeld YJ; Fisher A; Odibo AO; Haak MC; Borrell A
Ultrasound Obstet Gynecol; 2015 Dec; 46(6):650-8. PubMed ID: 25900824
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Clinical application of chromosomal microarray analysis in fetuses with increased nuchal translucency and normal karyotype.
Su L; Huang H; An G; Cai M; Wu X; Li Y; Xie X; Lin Y; Wang M; Xu L
Mol Genet Genomic Med; 2019 Aug; 7(8):e811. PubMed ID: 31209990
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. Relevance of Copy Number Variation at Chromosome X in Male Fetuses Inherited from the Mother May Be Ascertained by Including Male Relatives from the Maternal Lineage in Addition to Trio Analyses.
Chen M; Wu WJ; Lee MH; Ku TH; Ma GC
Genes (Basel); 2020 Aug; 11(9):. PubMed ID: 32842633
[TBL] [Abstract][Full Text] [Related]
14. Diagnostic yield of chromosomal microarray analysis in fetuses with isolated increased nuchal translucency: a French multicenter study.
Egloff M; Hervé B; Quibel T; Jaillard S; Le Bouar G; Uguen K; Saliou AH; Valduga M; Perdriolle E; Coutton C; Coston AL; Coussement A; Anselem O; Missirian C; Bretelle F; Prieur F; Fanget C; Muti C; Jacquemot MC; Beneteau C; Le Vaillant C; Vekemans M; Salomon LJ; Vialard F; Malan V
Ultrasound Obstet Gynecol; 2018 Dec; 52(6):715-721. PubMed ID: 29027723
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. 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]
18. Whole-genome array CGH identifies pathogenic copy number variations in fetuses with major malformations and a normal karyotype.
D'Amours G; Kibar Z; Mathonnet G; Fetni R; Tihy F; Désilets V; Nizard S; Michaud JL; Lemyre E
Clin Genet; 2012 Feb; 81(2):128-41. PubMed ID: 21496010
[TBL] [Abstract][Full Text] [Related]
19. Copy number variants and fetal structural abnormalities in stillborn fetuses: A secondary analysis of the Stillbirth Collaborative Research Network study.
Workalemahu T; Dalton S; Son SL; Allshouse A; Carey AZ; Page JM; Blue NR; Thorsten V; Goldenberg RL; Pinar H; Reddy UM; Silver RM
BJOG; 2024 Jan; 131(2):157-162. PubMed ID: 37264725
[TBL] [Abstract][Full Text] [Related]
20. Chromosome Microarray Analysis and Exome Sequencing: Implementation in Prenatal Diagnosis of Fetuses with Digestive System Malformations.
Wang Y; Liu L; Fu F; Li R; Lei T; Huang R; Li D; Liao C
Genes (Basel); 2023 Sep; 14(10):. PubMed ID: 37895220
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
