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Fengchan Han
ORCID
Publication Activity (10 Years)
Years Active: 2020-2020
Publications (10 Years): 1
Top Topics
Transcription Factor
Genome Wide Identification
Top Venues
BMC medical genetics
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This page only lists publications with an associated author ORCID identifier.
Publications
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Bingxin Zhou
,
Lili Yu
,
Yan Wang
,
Wenjing Shang
,
Yi Xie
,
Xiong Wang
,
Fengchan Han
A novel mutation in TRIOBP gene leading to congenital deafness in a Chinese family.
BMC medical genetics
21 (1) (2020)