Detection of 22q11.2 microduplication by cell‐free DNA screening and chromosomal microarray in fetus with multiple anomalies-Reference-Cited by-同舟云学术

Detection of 22q11.2 microduplication by cell‐free DNA screening and chromosomal microarray in fetus with multiple anomalies

Published:2016-09-13 Issue:4 Volume:48 Page:530-532
ISSN:0960-7692
Container-title:Ultrasound in Obstetrics & Gynecology
language:en
Short-container-title:Ultrasound Obstet Gynecol

Author:

Wu W.‐J.¹²,Ma G.‐C.¹³⁴,Lin Y.‐S.⁵,Yeang C.‐H.⁶,Ni Y.‐H.⁷,Li W.‐C.⁸,Tsai H.‐D.²,Shur‐Fen Gau S.⁹¹⁰,Chen M.¹⁰¹¹¹²

Affiliation:

1. Department of Genomic Medicine and Center for Medical Genetics, Changhua Christian Hospital; and Department of Genomic Science and Technology Changhua Christian Hospital Healthcare System Changhua Taiwan

2. Department of Obstetrics and Gynecology Changhua Christian Hospital Changhua Taiwan

3. Institute of Biochemistry, Microbiology and Immunology Chung Shan Medical University Taichung Taiwan

4. Department of Medical Laboratory Science and Biotechnology Central Taiwan University of Science and Technology Taichung Taiwan

5. Welgene Biotechnology Company Nangang Business Park Taipei Taiwan

6. Institute of Statistical Science Academia Sinica Taipei Taiwan

7. Department of Pediatrics National Taiwan University Hospital and College of Medicine Taipei Taiwan

8. Department of Obstetrics and Gynecology Puli Christian Hospital Nantou Taiwan

9. Department of Psychiatry National Taiwan University Hospital and College of Medicine Taipei Taiwan

10. Department of Medical Genetics National Taiwan University Hospital Taipei Taiwan

11. Department of Obstetrics and Gynecology National Taiwan University Hospital and College of Medicine Taipei Taiwan

12. Department of Life Science Tunghai University Taichung Taiwan

Funder

Ministry of Science and Technology

Changhua Christian Hospital

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.15965

Reference6 articles.

1. Noninvasive Prenatal Diagnosis of a Fetal Microdeletion Syndrome

2. Noninvasive detection of fetal subchromosomal abnormalities by semiconductor sequencing of maternal plasma DNA

3. Genome-wide normalized score: a novel algorithm to detect fetal trisomy 21 during non-invasive prenatal testing

4. Late Abortion: A Comprehensive Review

5. Phenotypic heterogeneity in a family with a small atypical microduplication of chromosome 22q11.2 involving TBX1

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