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K Stephens

Showing results (101-110 of 214) with videos related to

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The Journal of Investigative Dermatology|March 1, 1997
Primers for exon-specific amplification of the KRT5 gene: identification of novel and recurrent mutations in epidermolysis bullosa simplex patientsK Stephens, P Ehrlich, M Weaver, et al.
Nature Genetics|September 1, 1996
Identification of NF1 mutations in both alleles of a dermal neurofibromaS Sawada, S Florell, S M Purandare, et al.
American Journal of Medical Genetics|December 31, 1997
Familial neurofibromatosis 1 microdeletions: cosegregation with distinct facial phenotype and early onset of cutaneous neurofibromataK A Leppig, P Kaplan, D Viskochil, et al.
The Physician and Sportsmedicine|July 12, 2016
The Longevity and Morbidity of College AthletesH W Olson, H J Montoye, H Sprague, et al.
American Journal of Human Genetics|January 1, 1989
The order of loci in the pericentric region of chromosome 17, based on evidence from physical and genetic breakpointsP R Fain, E Wright, H F Willard, et al.
European Journal of Human Genetics : EJHG|March 14, 2000
Refined mapping of the human serotonin transporter (SLC6A4) gene within 17q11 adjacent to the CPD and NF1 genesS Shen, S Battersby, M Weaver, et al.
Neurology|October 1, 1996
Nine families with the SCA3/Machado-Joseph disease type of inherited ataxiaP E Greenstein, D Moore, E Levy-Lohad, et al.
Human Molecular Genetics|December 10, 1999
NF1 microdeletion breakpoints are clustered at flanking repetitive sequencesM O Dorschner, V P Sybert, M Weaver, et al.
Journal of Medical Genetics|October 1, 1992
Large de novo DNA deletion in a patient with sporadic neurofibromatosis 1, mental retardation, and dysmorphismL M Kayes, V M Riccardi, W Burke, et al.
Health Communication|February 11, 2015
Sharing Health Information and Influencing Behavioral Intentions: The Role of Health Literacy, Information Overload, and the Internet in the Diffusion of Healthy Heart InformationBrittani Crook, Keri K Stephens, Angie E Pastorek, et al.
Pageof 22

Showing results (101-110 of 214) with videos related to

Sort By:
Pageof 22
The Journal of Investigative Dermatology|March 1, 1997
Primers for exon-specific amplification of the KRT5 gene: identification of novel and recurrent mutations in epidermolysis bullosa simplex patientsK Stephens, P Ehrlich, M Weaver, et al.
Nature Genetics|September 1, 1996
Identification of NF1 mutations in both alleles of a dermal neurofibromaS Sawada, S Florell, S M Purandare, et al.
American Journal of Medical Genetics|December 31, 1997
Familial neurofibromatosis 1 microdeletions: cosegregation with distinct facial phenotype and early onset of cutaneous neurofibromataK A Leppig, P Kaplan, D Viskochil, et al.
The Physician and Sportsmedicine|July 12, 2016
The Longevity and Morbidity of College AthletesH W Olson, H J Montoye, H Sprague, et al.
American Journal of Human Genetics|January 1, 1989
The order of loci in the pericentric region of chromosome 17, based on evidence from physical and genetic breakpointsP R Fain, E Wright, H F Willard, et al.
European Journal of Human Genetics : EJHG|March 14, 2000
Refined mapping of the human serotonin transporter (SLC6A4) gene within 17q11 adjacent to the CPD and NF1 genesS Shen, S Battersby, M Weaver, et al.
Neurology|October 1, 1996
Nine families with the SCA3/Machado-Joseph disease type of inherited ataxiaP E Greenstein, D Moore, E Levy-Lohad, et al.
Human Molecular Genetics|December 10, 1999
NF1 microdeletion breakpoints are clustered at flanking repetitive sequencesM O Dorschner, V P Sybert, M Weaver, et al.
Journal of Medical Genetics|October 1, 1992
Large de novo DNA deletion in a patient with sporadic neurofibromatosis 1, mental retardation, and dysmorphismL M Kayes, V M Riccardi, W Burke, et al.
Health Communication|February 11, 2015
Sharing Health Information and Influencing Behavioral Intentions: The Role of Health Literacy, Information Overload, and the Internet in the Diffusion of Healthy Heart InformationBrittani Crook, Keri K Stephens, Angie E Pastorek, et al.
Pageof 22