Kunst HP - Search Results

1

De Leenheer EM, Ensink RJ, Kunst HP, Marres HA, Talebizadeh Z, Declau F, Smith SD, Usami S, Van de Heyning PH, Van Camp G, Huygen PL, Cremers CW. De Leenheer EM, et al. Among authors: kunst hp. Adv Otorhinolaryngol. 2002;61:41-6. doi: 10.1159/000066802. Adv Otorhinolaryngol. 2002. PMID: 12408061 No abstract available.

2

Linkage analysis of progressive hearing loss in five extended families maps the DFNA2 gene to a 1.25-Mb region on chromosome 1p.

Van Camp G, Coucke PJ, Kunst H, Schatteman I, Van Velzen D, Marres H, van Ewijk M, Declau F, Van Hauwe P, Meyers J, Kenyon J, Smith SD, Smith RJ, Djelantik B, Cremers CW, Van de Heyning PH, Willems PJ. Van Camp G, et al. Genomics. 1997 Apr 1;41(1):70-4. doi: 10.1006/geno.1997.4624. Genomics. 1997. PMID: 9126484 Free article.

3

Inherited nonsyndromic hearing loss. An audiovestibular study in a large family with autosomal dominant progressive hearing loss related to DFNA2.

Marres H, van Ewijk M, Huygen P, Kunst H, van Camp G, Coucke P, Willems P, Cremers C. Marres H, et al. Arch Otolaryngol Head Neck Surg. 1997 Jun;123(6):573-7. doi: 10.1001/archotol.1997.01900060015002. Arch Otolaryngol Head Neck Surg. 1997. PMID: 9193215 Free article.

4

Nonsyndromic autosomal dominant progressive sensorineural hearing loss: audiologic analysis of a pedigree linked to DFNA2.

Kunst H, Marres H, Huygen P, Ensink R, Van Camp G, Van Hauwe P, Coucke P, Willems P, Cremers C. Kunst H, et al. Laryngoscope. 1998 Jan;108(1 Pt 1):74-80. doi: 10.1097/00005537-199801000-00014. Laryngoscope. 1998. PMID: 9432071

5

Non-syndromic autosomal dominant sensorineural hearing loss: a new field of research.

Kunst H, Marres H, Van Camp G, Cremers C. Kunst H, et al. Clin Otolaryngol Allied Sci. 1998 Feb;23(1):9-17. doi: 10.1046/j.1365-2273.1998.00093.x. Clin Otolaryngol Allied Sci. 1998. PMID: 9563659 Review. No abstract available.

6

Deafness linked to DFNA2: one locus but how many genes?

Van Hauwe P, Coucke PJ, Declau F, Kunst H, Ensink RJ, Marres HA, Cremers CW, Djelantik B, Smith SD, Kelley P, Van de Heyning PH, Van Camp G. Van Hauwe P, et al. Nat Genet. 1999 Mar;21(3):263. doi: 10.1038/6778. Nat Genet. 1999. PMID: 10080176 No abstract available.

7

Mutations in the KCNQ4 gene are responsible for autosomal dominant deafness in four DFNA2 families.

Coucke PJ, Van Hauwe P, Kelley PM, Kunst H, Schatteman I, Van Velzen D, Meyers J, Ensink RJ, Verstreken M, Declau F, Marres H, Kastury K, Bhasin S, McGuirt WT, Smith RJ, Cremers CW, Van de Heyning P, Willems PJ, Smith SD, Van Camp G. Coucke PJ, et al. Hum Mol Genet. 1999 Jul;8(7):1321-8. doi: 10.1093/hmg/8.7.1321. Hum Mol Genet. 1999. PMID: 10369879

8

A gene for autosomal dominant hearing impairment (DFNA14) maps to a region on chromosome 4p16.3 that does not overlap the DFNA6 locus.

Van Camp G, Kunst H, Flothmann K, McGuirt W, Wauters J, Marres H, Verstreken M, Bespalova IN, Burmeister M, Van de Heyning PH, Smith RJ, Willems PJ, Cremers CW, Lesperance MM. Van Camp G, et al. J Med Genet. 1999 Jul;36(7):532-6. J Med Genet. 1999. PMID: 10424813 Free PMC article.

9

Autosomal dominant non-syndromal low-frequency sensorineural hearing impairment linked to chromosome 4p16 (DFNA14): statistical analysis of hearing threshold in relation to age and evaluation of vestibulo-ocular functions.

Kunst H, Marres H, Huygen P, Van Camp G, Joosten F, Cremers C. Kunst H, et al. Audiology. 1999 May-Jun;38(3):165-73. doi: 10.3109/00206099909073018. Audiology. 1999. PMID: 10437687 Review.

10

Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13).

McGuirt WT, Prasad SD, Griffith AJ, Kunst HP, Green GE, Shpargel KB, Runge C, Huybrechts C, Mueller RF, Lynch E, King MC, Brunner HG, Cremers CW, Takanosu M, Li SW, Arita M, Mayne R, Prockop DJ, Van Camp G, Smith RJ. McGuirt WT, et al. Among authors: kunst hp. Nat Genet. 1999 Dec;23(4):413-9. doi: 10.1038/70516. Nat Genet. 1999. PMID: 10581026

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