Hu Z - Search Results

1

Phenotype-to-genotype approach reveals head-circumference-associated genes in an autism spectrum disorder cohort.

Wu H, Li H, Bai T, Han L, Ou J, Xun G, Zhang Y, Wang Y, Duan G, Zhao N, Chen B, Du X, Yao M, Zou X, Zhao J, Hu Z, Eichler EE, Guo H, Xia K. Wu H, et al. Among authors: hu z. Clin Genet. 2020 Feb;97(2):338-346. doi: 10.1111/cge.13665. Epub 2019 Nov 14. Clin Genet. 2020. PMID: 31674007 Free PMC article.

2

[A mutation IVS2+1G>A in EXT2 gene causes hereditary multiple exostoses].

Hu ZM, Zheng D, Pan Q, Yang YF, Zhao TL, Liu XP, Wu LQ, Jiang DG, Xia K, Xia JH. Hu ZM, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004 Apr;21(2):97-100. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004. PMID: 15079787 Chinese.

3

A novel PRPF31 splice-site mutation in a Chinese family with autosomal dominant retinitis pigmentosa.

Xia K, Zheng D, Pan Q, Liu Z, Xi X, Hu Z, Deng H, Liu X, Jiang D, Deng H, Xia J. Xia K, et al. Among authors: hu z. Mol Vis. 2004 May 20;10:361-5. Mol Vis. 2004. PMID: 15162096 Free article.

4

[Mutation analysis of ganglioside-induced differentiation associated protein-1 gene in Chinese Charcot-Marie-Tooth disease].

Zhang RX, Tang BS, Zi XH, Luo W, Xia K, Pan Q, Long ZG, Hu ZM, Li XB. Zhang RX, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004 Jun;21(3):207-10. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004. PMID: 15192818 Chinese.

5

Confirmation and refinement of a genetic locus of congenital motor nystagmus in Xq26.3-q27.1 in a Chinese family.

Zhang B, Xia K, Ding M, Liang D, Liu Z, Pan Q, Hu Z, Wu LQ, Cai F, Xia J. Zhang B, et al. Among authors: hu z. Hum Genet. 2005 Jan;116(1-2):128-31. doi: 10.1007/s00439-004-1188-5. Epub 2004 Oct 23. Hum Genet. 2005. PMID: 15517395

6

[Mutation analysis of keratin 9 gene in a pedigree with epidermolytic palmoplantar keratoderma].

Zhang BR, Yin XZ, Xia K, Ding MP, Hu ZM, Zheng M, Liu ZR, Xia JH. Zhang BR, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004 Dec;21(6):570-3. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004. PMID: 15583984 Chinese.

7

[Mutation screening in selected exons of myosin 7a gene in prelingual non-syndromic hearing impairment patients].

Hu P, Xie DH, Xiao ZA, Wu WJ, Ge SL, Hu ZM, Xia K. Hu P, et al. Zhonghua Er Bi Yan Hou Ke Za Zhi. 2004 Sep;39(9):538-42. Zhonghua Er Bi Yan Hou Ke Za Zhi. 2004. PMID: 15606003 Chinese.

8

[Mapping of a pedigree with congenital nystagmus].

Liu ZR, Zhang BR, Ding MP, Xia K, Hu ZM, Deng H, Xia JH. Liu ZR, et al. Yi Chuan. 2004 Jul;26(4):437-40. Yi Chuan. 2004. PMID: 15640035 Chinese.

9

[ATM gene mutations in Chinese patients with ataxia telangiectasia].

Jiang H, Tang B, Hu Z, Xia K, Xu B, Tang J, Shen L. Jiang H, et al. Among authors: hu z. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Apr;22(2):121-4. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005. PMID: 15793768 Chinese.

10

[Studies on PANK2 gene mutations in Chinese patients with Hallervorden-Spatz syndrome].

Zhang Y, Tang B, Guo J, Long Z, Xia K, Pan Q, Hu Z, Wu D, Tang J, Chen T, Yan X. Zhang Y, et al. Among authors: hu z. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Apr;22(2):189-91. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005. PMID: 15793782 Chinese.

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