Ghent University Academic Bibliography

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- Journal Article
- A1
A novel DFNA5 mutation does not cause hearing loss in an Iranian family

Lut Van Laer (UGent) , NC Meyer, M Malekpour, Y Riazalhosseini, M Moghannibashi, K Kahrizi, A Vandevelde, F Alasti, H Najmabadi, G Van Camp, et al.

(2007) JOURNAL OF HUMAN GENETICS. 52(6). p.549-552
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- Journal Article
- A1
The coding polymorphism T263I in TGF-beta 1 is associated with otosclerosis in two independent populations

M THYS, I SCHRAUWEN, K VANDERSTRAETEN, K JANSSENS, N DIELTJENS, K VAN DEN BOGAERT, E FRANSEN, W CHEN, M EALY, M CLAUSTRES, et al.

(2007) HUMAN MOLECULAR GENETICS. 16(17). p.2021-2030
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- Journal Article
- A1
Mice lacking Dfna5 show a diverging number of cochlear fourth row outer hair cells

Lut Van Laer (UGent) , M Pfister, S Thys, K Vrijens, M Mueller, L Umans, L Serneels, L Van Nassauw, F Kooy, RJH Smith, et al.

(2005) NEUROBIOLOGY OF DISEASE. 19(3). p.386-399
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- Journal Article
- A1
DFNA5: hearing impairment exon instead of hearing impairment gene?

Lut Van Laer (UGent) , K Vrijens, S Thys, VFI Van Tendeloo, RJH Smith, DR Van Bockstaele, JP Timmermans and G Van Camp

(2004) JOURNAL OF MEDICAL GENETICS. 41(6). p.401-406
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- Journal Article
- A1
Nonsyndromic hearing loss

Lut Van Laer (UGent) , K Cryns, RJH Smith and G Van Camp

(2003) EAR AND HEARING. 24(4). p.275-288
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- Journal Article
- A1
The WFS1 gene, responsible for low frequency sensorineural hearing loss and Wolfram syndrome, is expressed in a variety of inner ear cells

K Cryns, S Thys, Lut Van Laer (UGent) , Y Oka, M Pfister, L Van Nassauw, RJH Smith, JP Timmermans and G Van Camp

(2003) HISTOCHEMISTRY AND CELL BIOLOGY. 119(3). p.247-256
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- Journal Article
- A1
- open access
A common founder for the 35delG GJB2 gene mutation in connexin 26 hearing impairment

Lut Van Laer (UGent) , Paul Coucke (UGent) , RF Mueller, G Caethoven, K Flothmann, SD Prasad, GP Chamberlin, M Houseman, GR Taylor, CM Van de Heyning, et al.

(2001) JOURNAL OF MEDICAL GENETICS. 38(8). p.515-518
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- Journal Article
- A1
Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F

KN Alagramam, HJ Yuan, MH Kuehn, CL Murcia, S Wayne, CRS Srisailpathy, RB Lowry, R Knaus, Lut Van Laer (UGent) , FP Bernier, et al.

(2001) HUMAN MOLECULAR GENETICS. 10(16). p.1709-1718
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- Journal Article
- A1
Autosomal recessive nonsyndromic hearing loss

RA Sundstrom, Lut Van Laer (UGent) , G Van Camp and RJH Smith

(1999) AMERICAN JOURNAL OF MEDICAL GENETICS. 89(3). p.123-129
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- Journal Article
- A1
Autosomal dominant nonsyndromic hearing impairment

Lut Van Laer (UGent) , WT McGuirt, T Yang, RJH Smith and G Van Camp

(1999) AMERICAN JOURNAL OF MEDICAL GENETICS. 89(3). p.167-174

Academic Bibliography

A novel DFNA5 mutation does not cause hearing loss in an Iranian family

The coding polymorphism T263I in TGF-beta 1 is associated with otosclerosis in two independent populations

Mice lacking Dfna5 show a diverging number of cochlear fourth row outer hair cells

DFNA5: hearing impairment exon instead of hearing impairment gene?

Nonsyndromic hearing loss

The WFS1 gene, responsible for low frequency sensorineural hearing loss and Wolfram syndrome, is expressed in a variety of inner ear cells

A common founder for the 35delG GJB2 gene mutation in connexin 26 hearing impairment

Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F

Autosomal recessive nonsyndromic hearing loss

Autosomal dominant nonsyndromic hearing impairment

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