5 results on '"Lu, Xiaomei"'
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2. A novel variant in the CDH23 gene is associated with non-syndromic hearing loss in a Chinese family
3. A novel mutation in the MYO7A gene is associated with Usher syndrome type 1 in a Chinese family
4. A novel missense mutation in the SLC26A4 gene causes nonsyndromic hearing loss and enlarged vestibular aqueduct
5. A novel nonsense mutation in the TCOF1 gene in one Chinese newborn with Treacher Collins syndrome
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