W. Shu

发表

Cutaneomucosal venous malformations are linked to the TIE2 mutation in a large Chinese family

Zihua Hu, Youkun Lin, Rong Hua, 2012, Experimental dermatology.

[Haplotype analysis for mucocutaneous venous malformations in a Chinese Han ethnic family].

Youkun Lin, Qi-Ping Hu, Rong Hua, 2012, Yi chuan = Hereditas.

Fluorescence In situ Hybridization: Cell-Based Genetic Diagnostic and Research Applications

Peining Li, Chenghua Cui, Peining Li, 2016, Front. Cell Dev. Biol..

The Spectrum of Cytogenomic Abnormalities in Patients with Developmental Delay and Intellectual Disabilities

Fang Xu, Peining Li, W. Shu, 2016 .

[Gene diagnosis and CAG repeat analysis of spinocerebellar ataxia cases of Guangxi region].

Ping Wang, Qi-Ping Hu, Rong Hua, 2009, Yi chuan = Hereditas.

A novel compound heterozygous mutation of K494_V495 deletion plus R496L and D487_F489 deletion in extreme C-terminus of cytochrome P450c17 causes 17α-hydroxylase deficiency

Chaur-Jong Hu, B. Chung, Su-Mei Chen, 2006, Molecular and Cellular Endocrinology.

A novel compound heterozygous mutation of K494_V495 deletion plus R496L and D487_F489 deletion in extreme C-terminus of cytochrome P450c17 causes 17alpha-hydroxylase deficiency.

Chaur-Jong Hu, B. Chung, Su-Mei Chen, 2006, Molecular and cellular endocrinology.

Human ring chromosome registry for cases in the Chinese population: re-emphasizing Cytogenomic and clinical heterogeneity and reviewing diagnostic and treatment strategies

Peining Li, Q. Hu, Hongyan Chai, 2018, Molecular Cytogenetics.

Cutaneomucosal venous malformations are linked to the TIE2 mutation in a large Chinese family

Zihua Hu, Youkun Lin, Rong Hua, 2012, Experimental dermatology.

Human ring chromosome registry for cases in the Chinese population: re-emphasizing Cytogenomic and clinical heterogeneity and reviewing diagnostic and treatment strategies

Peining Li, Q. Hu, Hongyan Chai, 2018, Molecular Cytogenetics.