A report on seven fetal cases associated with 15q11‐q13 microdeletion and microduplication-Reference-Cited by-同舟云学术

A report on seven fetal cases associated with 15q11‐q13 microdeletion and microduplication

Published:2021-02-04 Issue:3 Volume:9 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol. Genet. Genomic Med.

Author:

Huang Xiuzhu¹²,Chen Jieping²,Hu Wenlong²,Li Lu¹²,He Huiyan²,Guo Hui²,Liao Qiuyan²,Ye Mei²,Tang Donge²,Dai Yong²^ORCID

Affiliation:

1. MOE Key Laboratory of Tumor Molecular Biology and Key Laboratory of Functional Protein Research of Guangdong Higher Education Institutes Institute of Life and Health Engineering, College of Life Science and Technology Jinan University Guangzhou China

2. Clinical Medical Research Center The Second Clinical Medical College of Jinan University (Shenzhen People’s Hospital) Shenzhen China

Funder

Natural Science Foundation of Guangdong Province

Publisher

Wiley

Subject

Genetics(clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.1605

Reference27 articles.

1. Chromosome Breakage in the Prader-Willi and Angelman Syndromes Involves Recombination between Large, Transcribed Repeats at Proximal and Distal Breakpoints

2. Prader-Willi syndrome: a review of clinical, genetic, and endocrine findings

3. Highly restricted deletion of the SNORD116 region is implicated in Prader–Willi Syndrome

4. Prader–Willi syndrome: clinical genetics, cytogenetics and molecular biology

5. The human gene for the poly(A)-specific ribonuclease (PARN) maps to 16p13 and has a truncated copy in the Prader-Willi/Angelman syndrome region on 15q11→q13

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1. Prenatal diagnosis of 15q11.2 microdeletion fetuses in Eastern China: 21 case series and literature review;The Journal of Maternal-Fetal & Neonatal Medicine;2023-09-28

2. Prader–Willi Syndrome and Chromosome 15q11.2 BP1-BP2 Region: A Review;International Journal of Molecular Sciences;2023-02-21

3. Clinical and genetic study of three families with 15q11q13 duplications;Taiwanese Journal of Obstetrics and Gynecology;2022-07