Similar articles for PMID: 9106521

Year	Number of Results
1989	1
1990	2
1992	1
1994	3
1995	4
1996	7
1997	5
1998	11
1999	7
2000	16
2001	5
2002	7
2003	8
2004	6
2005	2
2006	3
2007	3
2008	1
2023	1
2024	0

1

Nonsyndromic hearing impairment: unparalleled heterogeneity.

Van Camp G, Willems PJ, Smith RJ. Van Camp G, et al. Am J Hum Genet. 1997 Apr;60(4):758-64. Am J Hum Genet. 1997. PMID: 9106521 Free PMC article. Review. No abstract available.

2

A new nonsyndromic X-linked sensorineural hearing impairment linked to Xp21.2.

Lalwani AK, Brister JR, Fex J, Grundfast KM, Pikus AT, Ploplis B, San Agustin T, Skarka H, Wilcox ER. Lalwani AK, et al. Am J Hum Genet. 1994 Oct;55(4):685-94. Am J Hum Genet. 1994. PMID: 7942846 Free PMC article.

3

Characterization of autosomal dominant non-syndromic hearing loss loci: DFNA 4, 6, 10 and 13.

McGuirt WT, Lesperance MM, Wilcox ER, Chen AH, Van Camp G, Smith RJ. McGuirt WT, et al. Adv Otorhinolaryngol. 2000;56:84-96. doi: 10.1159/000059085. Adv Otorhinolaryngol. 2000. PMID: 10868218 Review. No abstract available.

4

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. J Hum Genet. 2002;47(12):635-40. doi: 10.1007/s100380200098. J Hum Genet. 2002. PMID: 12522684

5

[Gene mapping of a nonsyndromic hearing impairmint family].

Cheng L, Gong Y, Liu Q, Chen B, Guo C, Li J, Zhang X, Lu Y, Gao G, Zhou H, Guo Y. Cheng L, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2003 Apr;20(2):89-93. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2003. PMID: 12673573 Chinese.

6

Evidence for digenic inheritance of nonsyndromic hereditary hearing loss in a Swedish family.

Balciuniene J, Dahl N, Borg E, Samuelsson E, Koisti MJ, Pettersson U, Jazin EE. Balciuniene J, et al. Am J Hum Genet. 1998 Sep;63(3):786-93. doi: 10.1086/302012. Am J Hum Genet. 1998. PMID: 9718342 Free PMC article.

7

Sensorineural hearing impairment non-syndromic, dominant DFNA11.

Tamagawa Y, Kitamura K, Ishida T, Nishizawa M, Liu XZ, Walsh J, Steel KP, Brown SD. Tamagawa Y, et al. Adv Otorhinolaryngol. 2000;56:103-6. doi: 10.1159/000059092. Adv Otorhinolaryngol. 2000. PMID: 10868221 No abstract available.

8

A second family with nonsyndromic sensorineural hearing loss linked to Xp21.2: refinement of the DFN4 locus within DMD.

Pfister MH, Apaydin F, Turan O, Bereketoglu M, Bylgen V, Braendle U, Zenner HP, Lalwani AK. Pfister MH, et al. Genomics. 1998 Nov 1;53(3):377-82. doi: 10.1006/geno.1998.5538. Genomics. 1998. PMID: 9799605

9

DFNB39, a recessive form of sensorineural hearing impairment, maps to chromosome 7q11.22-q21.12.

Wajid M, Abbasi AA, Ansar M, Pham TL, Yan K, Haque S, Ahmad W, Leal SM. Wajid M, et al. Eur J Hum Genet. 2003 Oct;11(10):812-5. doi: 10.1038/sj.ejhg.5201041. Eur J Hum Genet. 2003. PMID: 14512973 Free PMC article.

10

An autosomal recessive nonsyndromic form of sensorineural hearing loss maps to 3p-DFNB6.

Fukushima K, Ramesh A, Srisailapathy CR, Ni L, Wayne S, O'Neill ME, Van Camp G, Coucke P, Jain P, Wilcox ER, Smith SD, Kenyon JB, Zbar RI, Smith RJ. Fukushima K, et al. Genome Res. 1995 Oct;5(3):305-8. doi: 10.1101/gr.5.3.305. Genome Res. 1995. PMID: 8593615 Free article.

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