Yan Xu

2PUBLICATIONS
16CO-AUTHORS
Gene mapping
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Publications (2)

|May 20, 2026
Proband Nanopore Long-Read Genome Sequencing Facilitates Preimplantation Genetic Testing for Facioscapulohumeral Muscular Dystrophy.

|May 27, 2015
ALMS1 null mutations: a common cause of Leber congenital amaurosis and early-onset severe cone-rod dystrophy.

Y Xu, L Guan, X Xiao

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Frequent Collaborators

1 joint publications

Jiaojiao Wang

1 joint publications

Yixin Chen

1 joint publications

Yanhong Zeng

1 joint publications

Qiong Wang