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A T DeWan

Showing results (1-10 of 8) with videos related to

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Clinical Genetics|January 10, 2003
A second kindred linked to DFNA20 (17q25.3) reduces the genetic intervalA T DeWan, A R Parrado, S M Leal
Ophthalmic Genetics|January 3, 2001
Evidence for genetic heterogeneity in families with congenital motor nystagmus (CN)W S Oetting, C M Armstrong, A M Holleschau, et al.
Pediatric Obesity|November 19, 2014
Longitudinal associations between asthma and general and abdominal weight status among Norwegian adolescents and young adults: the HUNT StudyK B Egan, A S Ettinger, A T DeWan, et al.
American Journal of Human Genetics|December 15, 2000
A genome scan for renal function among hypertensives: the HyperGEN studyA T DeWan, D K Arnett, L D Atwood, et al.
Ophthalmic Genetics|July 13, 2001
Further refinement of the MYP2 locus for autosomal dominant high myopia by linkage disequilibrium analysisT L Young, L D Atwood, S M Ronan, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|January 28, 2017
Predictors of tanning dependence in white non-Hispanic females and malesB Cartmel, A E Bale, S T Mayne, et al.
American Journal of Human Genetics|September 19, 2003
Mutations in the gamma-actin gene (ACTG1) are associated with dominant progressive deafness (DFNA20/26)M Zhu, T Yang, S Wei, et al.
Human Molecular Genetics|November 16, 2001
Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing lossI N Bespalova, G Van Camp, S J Bom, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Clinical Genetics|January 10, 2003
A second kindred linked to DFNA20 (17q25.3) reduces the genetic intervalA T DeWan, A R Parrado, S M Leal
Ophthalmic Genetics|January 3, 2001
Evidence for genetic heterogeneity in families with congenital motor nystagmus (CN)W S Oetting, C M Armstrong, A M Holleschau, et al.
Pediatric Obesity|November 19, 2014
Longitudinal associations between asthma and general and abdominal weight status among Norwegian adolescents and young adults: the HUNT StudyK B Egan, A S Ettinger, A T DeWan, et al.
American Journal of Human Genetics|December 15, 2000
A genome scan for renal function among hypertensives: the HyperGEN studyA T DeWan, D K Arnett, L D Atwood, et al.
Ophthalmic Genetics|July 13, 2001
Further refinement of the MYP2 locus for autosomal dominant high myopia by linkage disequilibrium analysisT L Young, L D Atwood, S M Ronan, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|January 28, 2017
Predictors of tanning dependence in white non-Hispanic females and malesB Cartmel, A E Bale, S T Mayne, et al.
American Journal of Human Genetics|September 19, 2003
Mutations in the gamma-actin gene (ACTG1) are associated with dominant progressive deafness (DFNA20/26)M Zhu, T Yang, S Wei, et al.
Human Molecular Genetics|November 16, 2001
Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing lossI N Bespalova, G Van Camp, S J Bom, et al.
Pageof 1