Two novel mutations in the ANTXR2 gene in a Chinese patient suffering from hyaline fibromatosis syndrome: A case report-Reference-Cited by-同舟云学术

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Two novel mutations in the ANTXR2 gene in a Chinese patient suffering from hyaline fibromatosis syndrome: A case report

Published:2018-08-22 Issue: Volume: Page:
ISSN:1791-2997
Container-title:Molecular Medicine Reports
language:
Short-container-title:Mol Med Report

Author:

Gao Ying¹,Bai Jinli²,Wang Jiancai¹,Liu Xiaoyan¹

Affiliation:

1. Department of Dermatology, Capital Institute of Pediatrics, Peking University Teaching Hospital, Beijing 100020, P.R. China

2. Department of Medical Genetics, Capital Institute of Pediatrics, Peking University Teaching Hospital, Beijing 100020, P.R. China

Publisher

Spandidos Publications

Subject

Cancer Research,Oncology,Genetics,Molecular Biology,Molecular Medicine,Biochemistry

Cited by 3 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. Hyaline fibromatosis syndrome: a rare, yet recognizable syndrome;The Turkish Journal of Pediatrics;2024-05-23

2. Hyaline fibromatosis syndrome: a case presenting with gingival enlargement as the only clinical manifestation and a report of two new mutations in the ANTXR2 gene;BMC Oral Health;2021-10-09

3. Oral lesions containing amyloid-like material;Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology;2021-08

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