Hao Qiu

2PUBLICATIONS
1CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Neurogenetics
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Publications (2)

|May 13, 2024
FBXO11 variants are associated with intellectual disability and variable clinical manifestation in Chinese affected individuals.

Xin Pan, Li Liu, Xu Zhang

|Sep 04, 2019
Whole-exome sequencing identifies a donor splice-site variant in SMPX that causes rare X-linked congenital deafness.

Yuan Lv, Jia Gu, Hao Qiu

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Frequent Collaborators

1 joint publications

Caixia Liu