A novel splicing mutation of ARHGAP29 is associated with nonsyndromic cleft lip with or without cleft palate-Reference-Cited by-同舟云学术

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A novel splicing mutation of ARHGAP29 is associated with nonsyndromic cleft lip with or without cleft palate

Published:2020-07-22 Issue: Volume: Page:1-8
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:

Yu Qiuxia¹^ORCID,Deng Qiong¹,Fu Fang¹,Li Ru¹,Zhang Wenwen¹,Wan Junhui¹,Yang Xin¹,Wang Dan¹,Li Fucheng¹,Wu Shaoqing¹,Li Jian¹,Li Dongzhi¹,Liao Can¹

Affiliation:

1. Department of Prenatal Diagnostic Center, Guangzhou Women and Children’s Medical Center, Guangzhou Medical University, Guangzhou, P. R. China

Funder

the National Natural Science Foundation of China

Natural Science Foundation of Guangdong Province

Major Project of the Department of Science and Technology of Guangzhou

Publisher

Informa UK Limited

Subject

Obstetrics and Gynaecology,Pediatrics, Perinatology, and Child Health

Link

https://www.tandfonline.com/doi/pdf/10.1080/14767058.2020.1786523

Reference40 articles.

1. Identification of common non-coding variants at 1p22 that are functional for non-syndromic orofacial clefting

2. Cleft lip and palate: understanding genetic and environmental influences

3. Genetic Causes of Nonsyndromic Cleft Lip with or without Cleft Palate

4. Polymorphisms in genes involved in folate metabolism and orofacial clefts

5. Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24

Cited by 7 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. Four Loss of Function Pathogenic Variants in ARHGAP29 in Non-Syndromic Cleft Lip and Palate;2024-07-15

2. Exome sequencing improves genetic diagnosis of congenital orofacial clefts;Frontiers in Genetics;2023-09-07

3. GRHL2 and AP2a coordinate early surface ectoderm lineage commitment during development;iScience;2023-03

4. ARHGAP29 is required for keratinocyte proliferation and migration;2023-02-01

5. Application of exome sequencing for prenatal diagnosis of fetal structural anomalies: clinical experience and lessons learned from a cohort of 1618 fetuses;Genome Medicine;2022-10-28

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