Prenatal diagnosis of 15q11.2 microdeletion fetuses in Eastern China: 21 case series and literature review-Reference-Cited by-同舟云学术

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Prenatal diagnosis of 15q11.2 microdeletion fetuses in Eastern China: 21 case series and literature review

Published:2023-09-28 Issue:2 Volume:36 Page:
ISSN:1476-7058
Container-title:The Journal of Maternal-Fetal & Neonatal Medicine
language:en
Short-container-title:The Journal of Maternal-Fetal & Neonatal Medicine

Author:

Jiang Xia-Li¹,Liang Bin¹,Zhao Wan-Tong¹,Lin Na¹,Huang Hai-Long¹,Cai Mei-Ying¹,Xu Liang-Pu¹

Affiliation:

1. Medical Genetic Diagnosis and Therapy Center, Fujian Maternity and Child Health Hospital, Affifiliated Hospital of Fujian Medical University, Fujian Key Laboratory for Prenatal Diagnosis and Birth Defect, Fuzhou, China

Funder

the Fujian Provincial Natural Science Foundation

Fujian Provincial Health Technology

Publisher

Informa UK Limited

Subject

Obstetrics and Gynecology,Pediatrics, Perinatology and Child Health

Link

https://www.tandfonline.com/doi/pdf/10.1080/14767058.2023.2262700

Reference41 articles.

1. Genetic imprinting suggested by maternal heterodisomy in non-deletion Prader-Willi syndrome

2. Clinical and genetic aspects of Angelman syndrome

3. Truncating mutations of MAGEL2 cause Prader-Willi phenotypes and autism

4. Clinical and genetic aspects of the 15q11.2 BP1-BP2 microdeletion disorder

5. Prader-Willi, Angelman, and 15q11-q13 Duplication Syndromes

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