Utility of trio‐based prenatal exome sequencing incorporating splice‐site and mitochondrial genome assessment in pregnancies with fetal ultrasound anomalies: prospective cohort study-Reference-Cited by-同舟云学术

Utility of trio‐based prenatal exome sequencing incorporating splice‐site and mitochondrial genome assessment in pregnancies with fetal ultrasound anomalies: prospective cohort study

Published:2022-12 Issue:6 Volume:60 Page:780-792
ISSN:0960-7692
Container-title:Ultrasound in Obstetrics & Gynecology
language:en
Short-container-title:Ultrasound in Obstet & Gyne

Author:

Zhu X.¹^ORCID,Gao Z.¹,Wang Y.¹,Huang W.¹,Li Q.¹,Jiao Z.¹,Liu N.¹,Kong X.¹^ORCID

Affiliation:

1. Genetics and Prenatal Diagnosis Center, Department of Obstetrics and Gynecology The First Affiliated Hospital of Zhengzhou University Zhengzhou China

Funder

Ministry of Science and Technology of the People's Republic of China

Publisher

Wiley

Subject

Obstetrics and Gynecology,Radiology, Nuclear Medicine and imaging,Reproductive Medicine,General Medicine,Radiological and Ultrasound Technology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/uog.24974

Reference52 articles.

1. Annual Summary of Vital Statistics: 2012–2013

2. Annual Summary of Vital Statistics: 2013–2014

3. Update on overall prevalence of major birth defects – Atlanta, Georgia, 1978–2005;Centers for Disease Control and Prevention (CDC);MMWR Morb Mortal Wkly Rep,2008

4. Expert consensus on the application of low‐depth whole genome sequencing in prenatal diagnosis;Clinical Genetics Group Of Medical Genetics Branch Chinese Medical Association, Professional Committee For Prenatal Diagnosis Of Genetic Diseases Medical Genetics Branch Of Chinese Medical Association, Group Of Genetic Disease Prevention And Control Birth Defect Prevention And Control Committee Of Chinese Society Of Preventive Medcine;Zhonghua Yi Xue Yi Chuan Xue Za Zhi,2019

5. Chromosomal Microarray versus Karyotyping for Prenatal Diagnosis

Cited by 6 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Detection of genomic variants by genome sequencing in foetuses with central nervous system abnormalities;Annals of Medicine;2024-09-06

2. Molecular findings in patients for whole exome sequencing and mitochondrial genome assessment;Clinica Chimica Acta;2024-07

3. Prenatal exome sequencing for morphologically normal fetus: Should we be doing it?;Prenatal Diagnosis;2024-06-11

4. Prenatal Exome Sequencing Analysis in Fetuses with Various Ultrasound Findings;Journal of Clinical Medicine;2023-12-28

5. Molecular Findings Among Patients for Whole Exome Sequencing and mitochondrial genome assessment;2023-09-08