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Publications by Xiaofang Liang

Comprehensive Molecular Diagnosis of 67 Chinese Usher Syndrome Probands: High Rate of Ethnicity Specific Mutations in Chinese USH Patients

Orphanet Journal of Rare Diseases

English

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Novel Mutations in FKBP10 and PLOD2 Cause Rare Bruck Syndrome in Chinese Patients

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P2.13-46 Comprehensive Investigation of ERBB2 Transmembrane Domain Mutations (V659/G660) in 12,833 Chinese Lung Cancer Patients

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ASXL1 Mutations in Chinese Patients With Essential Thrombocythemia

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P1.03-28 Association Between Molecular Characteristics of CTNNB1 Mutations and Prognosis in Patients With NSCLC in Chinese Patients

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P2.03-08 Molecular Spectrum of Patients With MSH2 Mutations in Chinese Non-Small Cell Lung Cancer

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