Dai H - Search Results

1

A novel locus for autosomal dominant nonsyndromic hearing loss identified at 5q31.1-32 in a Chinese pedigree.

Xia J, Deng H, Feng Y, Zhang H, Pan Q, Dai H, Long Z, Tang B, Deng H, Chen Y, Zhang R, Zheng D, He Y, Xia K. Xia J, et al. Among authors: dai h. J Hum Genet. 2002;47(12):635-40. doi: 10.1007/s100380200098. J Hum Genet. 2002. PMID: 12522684

2

A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2L) maps to chromosome 12q24.

Tang BS, Luo W, Xia K, Xiao JF, Jiang H, Shen L, Tang JG, Zhao GH, Cai F, Pan Q, Dai HP, Yang QD, Xia JH, Evgrafov OV. Tang BS, et al. Among authors: dai hp. Hum Genet. 2004 May;114(6):527-33. doi: 10.1007/s00439-004-1102-1. Epub 2004 Mar 12. Hum Genet. 2004. PMID: 15021985

3

Small heat-shock protein 22 mutated in autosomal dominant Charcot-Marie-Tooth disease type 2L.

Tang BS, Zhao GH, Luo W, Xia K, Cai F, Pan Q, Zhang RX, Zhang FF, Liu XM, Chen B, Zhang C, Shen L, Jiang H, Long ZG, Dai HP. Tang BS, et al. Among authors: dai hp. Hum Genet. 2005 Feb;116(3):222-4. doi: 10.1007/s00439-004-1218-3. Epub 2004 Nov 23. Hum Genet. 2005. PMID: 15565283

4

[Mapping of pathogenic genes in a pedigree with autosomal dominant ichthyosis vulgaris].

Hu ZM, Xie ZG, Wu LQ, Liang DS, Zhu HY, Pan Q, Long ZG, Dai HP, Xia JH, Xia K. Hu ZM, et al. Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2007 Jun;29(3):302-6. Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2007. PMID: 17633452 Chinese.

5

Molecular analysis of hearing loss associated with enlarged vestibular aqueduct in the mainland Chinese: a unique SLC26A4 mutation spectrum.

Hu H, Wu L, Feng Y, Pan Q, Long Z, Li J, Dai H, Xia K, Liang D, Niikawa N, Xia J. Hu H, et al. Among authors: dai h. J Hum Genet. 2007;52(6):492-497. doi: 10.1007/s10038-007-0139-0. Epub 2007 Apr 19. J Hum Genet. 2007. PMID: 17443271

6

A syndactyly type IV locus maps to 7q36.

Sato D, Liang D, Wu L, Pan Q, Xia K, Dai H, Wang H, Nishimura G, Yoshiura KI, Xia J, Niikawa N. Sato D, et al. Among authors: dai h. J Hum Genet. 2007;52(6):561-564. doi: 10.1007/s10038-007-0150-5. Epub 2007 May 3. J Hum Genet. 2007. PMID: 17476456

7

Mutations in the gene encoding gap junction protein beta-3 associated with autosomal dominant hearing impairment.

Xia JH, Liu CY, Tang BS, Pan Q, Huang L, Dai HP, Zhang BR, Xie W, Hu DX, Zheng D, Shi XL, Wang DA, Xia K, Yu KP, Liao XD, Feng Y, Yang YF, Xiao JY, Xie DH, Huang JZ. Xia JH, et al. Among authors: dai hp. Nat Genet. 1998 Dec;20(4):370-3. doi: 10.1038/3845. Nat Genet. 1998. PMID: 9843210

8

Identification of a locus for disseminated superficial actinic porokeratosis at chromosome 12q23.2-24.1.

Xia JH, Yang YF, Deng H, Tang BS, Tang DS, He YG, Xia K, Chen SX, Li YX, Pan Q, Long ZG, Dai HP, Liao XD, Xiao JF, Liu ZR, Lu CY, Yu KP, Deng HX. Xia JH, et al. Among authors: dai hp. J Invest Dermatol. 2000 Jun;114(6):1071-4. doi: 10.1046/j.1523-1747.2000.00978.x. J Invest Dermatol. 2000. PMID: 10844547 Free article.

9

A novel locus (DSAP2) for disseminated superficial actinic porokeratosis maps to chromosome 15q25.1-26.1.

Xia K, Deng H, Xia JH, Zheng D, Zhang HL, Lu CY, Li CQ, Pan Q, Dai HP, Yang YF, Long ZG, Deng HX. Xia K, et al. Among authors: dai hp. Br J Dermatol. 2002 Oct;147(4):650-4. doi: 10.1046/j.1365-2133.2002.05058.x. Br J Dermatol. 2002. PMID: 12366408

10

Confirmation and refinement of a genetic locus for disseminated superficial actinic porokeratosis (DSAP1) at 12q23.2-24.1.

Wu LQ, Yang YF, Zheng D, Deng H, Pan Q, Zhao TL, Cai F, Feng Y, Long ZG, Dai HP, Tang BS, Yang YJ, Deng HX, Xia K, Xia JH. Wu LQ, et al. Among authors: dai hp. Br J Dermatol. 2004 May;150(5):999-1004. doi: 10.1111/j.1365-2133.2004.05912.x. Br J Dermatol. 2004. PMID: 15149516

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