Identification of a novel gross deletion of TCOF1 in a Chinese prenatal case with Treacher Collins syndrome-Reference-Cited by-同舟云学术

Identification of a novel gross deletion of TCOF1 in a Chinese prenatal case with Treacher Collins syndrome

Author:

Liu Jing¹²,Lin Pengsiyuan³,Pang Jialun¹²,Jia Zhengjun¹²,Peng Ying¹²^ORCID,Xi Hui¹²,Wu Lingqian³^ORCID,Li Zhuo³^ORCID,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. Center for Medical Genetics & Hunan Key Laboratory of Medical Genetics School of Life Sciences Central South University Changsha Hunan China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Genetics(clinical),Genetics,Molecular Biology

Link

Reference28 articles.

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