Search Results - Shuyang Gao
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A Heterozygous Novel Mutation in TFAP2A Gene Causes Atypical Branchio-Oculo-Facial Syndrome With Isolated Coloboma of Choroid: A Case Report by Jie Min, Bing Mao, Yong Wang, Xuelian He, Shuyang Gao, Hairong Wang
Published 2020Call Number: Loading…Connect to this object online.
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2
Novel compound heterozygous mutations in OCA2 gene associated with non-syndromic oculocutaneous albinism in a Chinese Han patient: a case report by Hairong Wang, Yang Wan, Yun Yang, Hao Li, Liangwei Mao, Shuyang Gao, Jingjing Xu, Jing Wang
Published 2019Call Number: Loading…Connect to this object online.
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