Clinical and molecular characterization of 12 prenatal cases of Cri‐du‐chat syndrome-Reference-Cited by-同舟云学术

Clinical and molecular characterization of 12 prenatal cases of Cri‐du‐chat syndrome

Published:2020-06-04 Issue:8 Volume:8 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Peng Ying¹²^ORCID,Pang Jialun¹²,Hu Jiancheng¹²,Jia Zhengjun¹²,Xi Hui¹²,Ma Na¹²,Yang Shuting¹²,Liu Jing¹²,Huang Xiaoliang¹²,Tang Chengyuan³,Wang Hua¹²

Affiliation:

1. Department of Medical Genetics Hunan Provincial Maternal and Child Health Care Hospital Changsha Hunan China

2. National Health Commission Key Laboratory of Birth Defects Research, Prevention and Treatment Changsha Hunan China

3. Department of Nephrology Hunan Key Laboratory of Kidney Disease and Blood Purification The Second Xiangya HospitalCentral South University Changsha Hunan China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.1312

Reference38 articles.

1. Aberrant methylation of t RNA s links cellular stress to neuro‐developmental disorders

2. Parent of Origin, Mosaicism, and Recurrence Risk: Probabilistic Modeling Explains the Broken Symmetry of Transmission Genetics

3. Cri du Chat syndrome

4. Cri-du-chat (5p-) syndrome presenting with cerebellar hypoplasia and hypospadias: Prenatal diagnosis and aCGH characterization using uncultured amniocytes

5. Integrated analysis of the critical region 5p15.3–p15.2 associated with cri-du-chat syndrome

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