McGuirt WT - Search Results

1

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.

2

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. Nat Genet. 1999 Dec;23(4):413-9. doi: 10.1038/70516. Nat Genet. 1999. PMID: 10581026

3

DFNB15: autosomal recessive non-syndromic hearing loss gene-chromosome 3q, 19p or digenic recessive inheritance?

Chen AH, Fukushima K, McGuirt WT, Smith RJ. Chen AH, et al. Among authors: mcguirt wt. Adv Otorhinolaryngol. 2000;56:171-5. doi: 10.1159/000059089. Adv Otorhinolaryngol. 2000. PMID: 10868231 No abstract available.

4

Clinical presentation of DFNB1.

McGuirt WT, Prasad SD, Cucci RA, Green GE, Smith RJ. McGuirt WT, et al. Adv Otorhinolaryngol. 2002;61:113-9. doi: 10.1159/000066821. Adv Otorhinolaryngol. 2002. PMID: 12408072 No abstract available.

5

Localization of a gene for otosclerosis to chromosome 15q25-q26.

Tomek MS, Brown MR, Mani SR, Ramesh A, Srisailapathy CR, Coucke P, Zbar RI, Bell AM, McGuirt WT, Fukushima K, Willems PJ, Van Camp G, Smith RJ. Tomek MS, et al. Among authors: mcguirt wt. Hum Mol Genet. 1998 Feb;7(2):285-90. doi: 10.1093/hmg/7.2.285. Hum Mol Genet. 1998. PMID: 9425236

6

A gene for fluctuating, progressive autosomal dominant nonsyndromic hearing loss, DFNA16, maps to chromosome 2q23-24.3.

Fukushima K, Kasai N, Ueki Y, Nishizaki K, Sugata K, Hirakawa S, Masuda A, Gunduz M, Ninomiya Y, Masuda Y, Sato M, McGuirt WT, Coucke P, Van Camp G, Smith RJ. Fukushima K, et al. Among authors: mcguirt wt. Am J Hum Genet. 1999 Jul;65(1):141-50. doi: 10.1086/302461. Am J Hum Genet. 1999. PMID: 10364526 Free PMC article.

7

Connexin 26 as a cause of hereditary hearing loss.

McGuirt WT, Smith RJ. McGuirt WT, et al. Am J Audiol. 1999 Dec;8(2):93-100. doi: 10.1044/1059-0889(1999/016). Am J Audiol. 1999. PMID: 10646192

8

Temporal bone histopathology in connexin 26-related hearing loss.

Jun AI, McGuirt WT, Hinojosa R, Green GE, Fischel-Ghodsian N, Smith RJ. Jun AI, et al. Among authors: mcguirt wt. Laryngoscope. 2000 Feb;110(2 Pt 1):269-75. doi: 10.1097/00005537-200002010-00016. Laryngoscope. 2000. PMID: 10680928

9

Autosomal dominant nonsyndromic hearing impairment.

Van Laer L, McGuirt WT, Yang T, Smith RJ, Van Camp G. Van Laer L, et al. Among authors: mcguirt wt. Am J Med Genet. 1999 Sep 24;89(3):167-74. doi: 10.1002/(sici)1096-8628(19990924)89:3<167::aid-ajmg7>3.3.co;2-m. Am J Med Genet. 1999. PMID: 10704191 Review.

10

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.

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