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T Fagerheim

Showing results (1-10 of 7) with videos related to

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Advances in Oto-Rhino-Laryngology|June 27, 2000
DFNA7L Tranebjaerg, H H Elverland, T Fagerheim
Journal of Medical Genetics|October 3, 1999
A new gene (DYX3) for dyslexia is located on chromosome 2T Fagerheim, P Raeymaekers, F E Tønnessen, et al.
Ophthalmic Genetics|January 3, 2001
Autosomal dominant cone-rod dystrophy due to a missense mutation (R838C) in the guanylate cyclase 2D gene (GUCY2D) with preserved rod function in one branch of the familyM Van Ghelue, H L Eriksen, V Ponjavic, et al.
Human Molecular Genetics|August 1, 1996
Identification of a new locus for autosomal dominant non-syndromic hearing impairment (DFNA7) in a large Norwegian familyT Fagerheim, O Nilssen, P Raeymaekers, et al.
Journal of Medical Genetics|March 2, 1999
Homozygosity mapping to the USH2A locus in two isolated populationsT Fagerheim, P Raeymaekers, J Merren, et al.
Clinical Genetics|January 23, 2013
SLC26A4 mutation frequency and spectrum in 109 Danish Pendred syndrome/DFNB4 probands and a report of nine novel mutationsN D Rendtorff, I Schrijver, M Lodahl, et al.
Human Genetics|September 12, 2000
Refined localization and two additional linked families for the DFNA10 locus for nonsyndromic hearing impairmentK Verhoeven, T Fagerheim, S Prasad, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Advances in Oto-Rhino-Laryngology|June 27, 2000
DFNA7L Tranebjaerg, H H Elverland, T Fagerheim
Journal of Medical Genetics|October 3, 1999
A new gene (DYX3) for dyslexia is located on chromosome 2T Fagerheim, P Raeymaekers, F E Tønnessen, et al.
Ophthalmic Genetics|January 3, 2001
Autosomal dominant cone-rod dystrophy due to a missense mutation (R838C) in the guanylate cyclase 2D gene (GUCY2D) with preserved rod function in one branch of the familyM Van Ghelue, H L Eriksen, V Ponjavic, et al.
Human Molecular Genetics|August 1, 1996
Identification of a new locus for autosomal dominant non-syndromic hearing impairment (DFNA7) in a large Norwegian familyT Fagerheim, O Nilssen, P Raeymaekers, et al.
Journal of Medical Genetics|March 2, 1999
Homozygosity mapping to the USH2A locus in two isolated populationsT Fagerheim, P Raeymaekers, J Merren, et al.
Clinical Genetics|January 23, 2013
SLC26A4 mutation frequency and spectrum in 109 Danish Pendred syndrome/DFNB4 probands and a report of nine novel mutationsN D Rendtorff, I Schrijver, M Lodahl, et al.
Human Genetics|September 12, 2000
Refined localization and two additional linked families for the DFNA10 locus for nonsyndromic hearing impairmentK Verhoeven, T Fagerheim, S Prasad, et al.
Pageof 1