遗传与出生缺陷疾病研究组

Laboratory of Inherited Disorders and Birth Defects

发表论文
1.

Zhong Z#, Yan M#, Sun W, Wu Z, Han L, Zhou Z, Zheng F*., Chen J*Two novel mutations in PRPF3 causing autosomal dominant retinitis pigmentosa. Sci Rep. 2016 Nov 25; 6:37840.

2.

Zhong Z, Zhong M, Lu Y, Lu L, Wang J, Xu D, Wang F, Xu G, Chen J*. Identification of mutations in U2HR in two Chinese families with Marie Unna hereditary hypotrichosis. Clin Exp Dermatol. 2016 Mar;41(2):175-8.

3.

Liao RF#, Zhong ZL#, Ye MJ, Han LY, Ye DQ*, Chen JJ. Identification of Mutations in Myocilin and Beta-1,4-galactosyltransferase 3 Genes in a Chinese Family with Primary Open-angle Glaucoma. Chin Med J (Engl). 2016 Dec 5;129(23):2810-2815.

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