Prenatally diagnosed de novo segmental amplification or deletion by microarray-based comparative genomic hybridization: A retrospective study-Reference-Cited by-同舟云学术

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Prenatally diagnosed de novo segmental amplification or deletion by microarray-based comparative genomic hybridization: A retrospective study

Published:2019-09 Issue:5 Volume:58 Page:662-666
ISSN:1028-4559
Container-title:Taiwanese Journal of Obstetrics and Gynecology
language:en
Short-container-title:Taiwanese Journal of Obstetrics and Gynecology

Author:

Peng Hsiu-Huei,Lee Chien-Hong,Su Sheng-Yuan,Chen Kuan-Ju,Lee Yen-Chang,You Shu-Han,Lee Wen-Fang,Cheng Po-Jen

Funder

Chang Gung Memorial Hospital

Publisher

Elsevier BV

Subject

Obstetrics and Gynecology

Reference21 articles.

1. Chromosomal microarray in prenatal diagnosis: case studies and clinical challenges;Karla Leavitt;Pers Med,2016

2. Prenatal diagnosis by chromosomal microarray analysis;Levy;Fertil Steril,2018

3. Routine use of array comparative genomic hybridization (aCGH) as standard approach for prenatal diagnosis of chromosomal abnormalities. Clinical experience of 1763 prenatal cases;Papoulidis;Prenat Diagn,2015

4. Clinical utility of array comparative genomic hybridisation for prenatal diagnosis: a cohort study of 3171 pregnancies;Lee;Bjog,2012

5. A de novo duplication of chromosome 9q34.13-qter in a fetus with tetralogy of Fallot syndrome;Liu;Mol Cytogenet,2016

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1. Investigating the significance of segmental aneuploidy findings in preimplantation embryos;F&S Science;2023-05

2. Molecular Approaches in Fetal Malformations, Dynamic Anomalies and Soft Markers: Diagnostic Rates and Challenges—Systematic Review of the Literature and Meta-Analysis;Diagnostics;2022-02-23

3. Adverse Perinatal and Early Life Outcomes following 15q11.2 CNV Diagnosis;Genes;2021-09-23

4. Introduce the outstanding research paper awards of the Taiwan Association of Obstetrics and Gynecology and Hsu Chien-Tien Cancer Foundation in 2020;Taiwanese Journal of Obstetrics and Gynecology;2020-07

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