Prenatal diagnosis of 913 fetuses samples using copy number variation sequencing-Reference-Cited by-同舟云学术

Prenatal diagnosis of 913 fetuses samples using copy number variation sequencing

Published:2021-03-21 Issue:5 Volume:23 Page:
ISSN:1099-498X
Container-title:The Journal of Gene Medicine
language:en
Short-container-title:J Gene Med

Author:

Lan Liubing¹²³,She Lingna¹⁴³,Zhang Bosen¹⁴³,He Yanhong¹²³,Zheng Zhiyuan¹³^ORCID

Affiliation:

1. Prenatal Diagnosis Center, Meizhou People's Hospital (Huangtang Hospital) Meizhou Hospital Affiliated to Sun Yat‐sen University Meizhou China

2. Department of Obstetrics, Meizhou People's Hospital (Huangtang Hospital) Meizhou Hospital Affiliated to Sun Yat‐sen University Meizhou China

3. Guangdong Provincial Key Laboratory of Precision Medicine and Clinical Translational Research of Hakka Population, Meizhou People's Hospital (Huangtang Hospital), Meizhou Academy of Medical Sciences Meizhou Hospital Affiliated to Sun Yat‐sen University Meizhou China

4. Ultrasonic Department, Meizhou People's Hospital (Huangtang Hospital) Meizhou Hospital Affiliated to Sun Yat‐sen University Meizhou China

Publisher

Wiley

Subject

Genetics (clinical),Drug Discovery,Genetics,Molecular Biology,Molecular Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jgm.3324

Reference18 articles.

1. Whole-genome array CGH identifies pathogenic copy number variations in fetuses with major malformations and a normal karyotype

2. Detection of genomic imbalances by array based comparative genomic hybridisation in fetuses with multiple malformations

3. New microdeletion and microduplication syndromes: a comprehensive review

4. Microdeletion and Microduplication Syndromes

5. Noninvasive prenatal screening or advanced diagnostic testing: caveat emptor

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1. Comparative Efficacy of CNV-Sequencing and Karyotyping in Prenatal Genetic Diagnosis;Biomedical Research and Therapy;2024-07-31

2. Retrospective study revealed integration of CNV-seq and karyotype analysis is an effective strategy for prenatal diagnosis of chromosomal abnormalities;Frontiers in Genetics;2024-05-23

3. A clinical study of CNV-seq techniques in 103 cases of spontaneous abortion;2024-05-10

4. Application of Copy Number Variation Sequencing Technology in 422 Foetuses with Abnormal Ultrasound Soft Markers;International Journal of Women's Health;2023-11

5. Chromosome abnormalities and copy number variations in fetuses with ultrasound soft markers: a retrospective study;2023-09-29