6 results on '"Wang, Xiong"'
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2. A novel mutation in TRIOBP gene leading to congenital deafness in a Chinese family
3. Alpha and beta-Thalassemia mutations in Hubei area of China
4. Novel NOG (p.P42S) mutation causes proximal symphalangism in a four-generation Chinese family
5. Exacerbation of ichthyosis vulgaris phenotype by co-inheritance of STS and FLG mutations in a Chinese family with ichthyosis: a case report
6. Hemophagocytic lymphohistiocytosis and congenital factor VII deficiency: a case report
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