Open AccessPrenatal diagnosis of Bardet‑Biedl syndrome due to novel variants in the BBS10 gene in a fetus with multiple anomalies: A case report
Author(s) -
Xingsheng Dong,
Zhiming Li,
Degang Wang,
Yi Xiong,
Haijun Li,
Pu Yang,
Lanyu Lao,
Tingting Man,
Yujie Gan
Publication year - 2022
Publication title -
experimental and therapeutic medicine
Language(s) - English
Resource type - Journals
eISSN - 1792-1015
pISSN - 1792-0981
DOI - 10.3892/etm.2022.11657
Subject(s) - bardet–biedl syndrome , prenatal diagnosis , molecular medicine , fetus , oncogene , gene , bioinformatics , genetics , medicine , biology , cell cycle , pregnancy , phenotype
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