181 related articles for article (PubMed ID: 35456496)
1. 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]
2. 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]
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. 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]
5. 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]
6. 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]
7. 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]
8. Experience of chromosomal microarray applied in prenatal and postnatal settings in Hong Kong.
Cheng SSW; Chan KYK; Leung KKP; Au PKC; Tam WK; Li SKM; Luk HM; Kan ASY; Chung BHY; Lo IFM; Tang MHY
Am J Med Genet C Semin Med Genet; 2019 Jun; 181(2):196-207. PubMed ID: 30903683
[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. Application of chromosomal microarray in fetuses with increased nuchal translucency.
Zhao XR; Gao L; Wu Y; Wang YL
J Matern Fetal Neonatal Med; 2020 May; 33(10):1749-1754. PubMed ID: 30688128
[No Abstract] [Full Text] [Related]
11. Chromosomal microarray analysis in fetuses with high-risk prenatal indications: A retrospective study in China.
Luo X; Zhu H; Wang L; Xiao B; Fan Y; Ye H; Ying X; Qiu W; Zhang H; Han L; Gu X; Yu Y; Wang L
Taiwan J Obstet Gynecol; 2021 Mar; 60(2):299-304. PubMed ID: 33678331
[TBL] [Abstract][Full Text] [Related]
12. [Fetal chromosome technique by microarray-based comparative genomic hybridization].
Jonveaux P
Arch Pediatr; 2010 Jul; 17(7):1119-23. PubMed ID: 20347579
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. Chromosomal microarray analysis in fetuses with aberrant right subclavian artery.
Maya I; Kahana S; Yeshaya J; Tenne T; Yacobson S; Agmon-Fishman I; Cohen-Vig L; Levi A; Reinstein E; Basel-Vanagaite L; Sharony R
Ultrasound Obstet Gynecol; 2017 Mar; 49(3):337-341. PubMed ID: 27063194
[TBL] [Abstract][Full Text] [Related]
16. Chromosomal microarray analysis as a first-line test in pregnancies with a priori low risk for the detection of submicroscopic chromosomal abnormalities.
Fiorentino F; Napoletano S; Caiazzo F; Sessa M; Bono S; Spizzichino L; Gordon A; Nuccitelli A; Rizzo G; Baldi M
Eur J Hum Genet; 2013 Jul; 21(7):725-30. PubMed ID: 23211699
[TBL] [Abstract][Full Text] [Related]
17. The Effect of Resolution Level and Targeted Design in the Diagnostic Performance of Prenatal Chromosomal Microarray Analysis.
Papageorgiou E; Athanasiadis A; Fidani S; Papoulidis I; Manolakos E; Siomou E; Chatzakis C; Sotiriadis A
Fetal Diagn Ther; 2023; 50(6):397-405. PubMed ID: 37549642
[TBL] [Abstract][Full Text] [Related]
18. Detection of submicroscopic chromosomal aberrations by chromosomal microarray analysis for the prenatal diagnosis of central nervous system abnormalities.
Song T; Xu Y; Li Y; Jia L; Zheng J; Dang Y; Wan S; Zheng Y; Zhang J; Yang H
J Clin Lab Anal; 2020 Oct; 34(10):e23434. PubMed ID: 32677110
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. [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]
[Next] [New Search]
