Applying high‐throughput sequencing to identify and evaluate foetal chromosomal deletion and duplication-Reference-Cited by-同舟云学术

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Applying high‐throughput sequencing to identify and evaluate foetal chromosomal deletion and duplication

Published:2020-07-15 Issue:17 Volume:24 Page:9936-9944
ISSN:1582-1838
Container-title:Journal of Cellular and Molecular Medicine
language:en
Short-container-title:J Cell Mol Med

Author:

Wu Yueli¹,Zhang Linlin²^ORCID,Lv Hong¹,Li Ying¹,Zhu Chongyang¹,Tian Weifang¹,Zhao Ling¹

Affiliation:

1. Prenatal Diagnosis Center of Henan Women and Children Hospital and Institute the Third Affiliated Hospital of Zhengzhou University Zhengzhou China

2. Clinical Laboratory of Henan Women and Children Hospital and Institute the Third Affiliated Hospital of Zhengzhou University Zhengzhou China

Publisher

Wiley

Subject

Cell Biology,Molecular Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/jcmm.15593

Reference28 articles.

1. An Update on Common Chromosome Microdeletion and Microduplication Syndromes

2. Cri-Du-Chat Syndrome: Clinical Profile and Chromosomal Microarray Analysis in Six Patients

3. 22q11.2 deletion syndrome

4. Noninvasive Prenatal Testing and Incidental Detection of Occult Maternal Malignancies

5. Prenatal Diagnosis

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2. Clinical, Cytogenetic and Molecular Cytogenetic Outcomes of Cell-Free DNA Testing for Rare Chromosomal Anomalies;Genes;2022-12-16

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4. Current Perspectives of Prenatal Cell-free DNA Screening in Clinical Management of First-Trimester Septated Cystic Hygroma;International Journal of Women's Health;2022-10

5. Prenatal diagnosis of chromosome 18 long arm deletion syndrome by high-throughput sequencing;Medicine;2021-12-17

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