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American Journal of Human Genetics
|
October 6, 2000
Mutation in the gene for connexin 30.3 in a family with erythrokeratodermia variabilis
F Macari, M Landau, P Cousin, et al.
The British Journal of Dermatology
|
June 12, 2008
Simultaneous manifestation of variegate porphyria in monozygotic twins
L Borradori, A-M Van Tuyll van Serooskerken, S Abraham, et al.
Differentiation; Research in Biological Diversity
|
August 1, 1993
Expression patterns of loricrin in various species and tissues
D Hohl, B Ruf Olano, P A de Viragh, et al.
Supportive Care in Cancer : Official Journal of the Multinational Association of Supportive Care in Cancer
|
August 26, 2016
Exploring the role of physician communication about adjuvant endocrine therapy among breast cancer patients on active treatment: a qualitative analysis
Albert J Farias, India J Ornelas, Sarah D Hohl, et al.
Experimental Dermatology
|
August 10, 1999
Hair shaft defects visualized after detergent extraction
R H Rice, V J Wong, M L Williams, et al.
Preventive Medicine Reports
|
July 22, 2022
Multi-component interventions and change in screening rates in primary care clinics in the Colorectal Cancer Control Program
Krishna P Sharma, Amy DeGroff, Sarah D Hohl, et al.
The British Journal of Dermatology
|
August 21, 2013
Identification of the first nonsense CDSN mutation with expression of a truncated protein causing peeling skin syndrome type B
A Mallet, M Kypriotou, K George, et al.
Progress in Community Health Partnerships : Research, Education, and Action
|
June 2, 2017
Engaging Study Participants in Research Dissemination at a Center for Population Health and Health Disparities
Sarah Knerr, Sarah D Hohl, Yamile Molina, et al.
The Journal of Investigative Dermatology
|
April 14, 1999
A novel substitution in keratin 10 in epidermolytic hyperkeratosis
M J Arin, M A Longley, I Anton-Lamprecht, et al.
Nature Genetics
|
August 1, 1994
Mutations in the rod domain of keratin 2e in patients with ichthyosis bullosa of Siemens
J A Rothnagel, H Traupe, S Wojcik, et al.
Page
of 15
Search research articles
Search
Showing results (91-100 of 144) with videos related to
Sort By:
Page
of 15
American Journal of Human Genetics
|
October 6, 2000
Mutation in the gene for connexin 30.3 in a family with erythrokeratodermia variabilis
F Macari, M Landau, P Cousin, et al.
The British Journal of Dermatology
|
June 12, 2008
Simultaneous manifestation of variegate porphyria in monozygotic twins
L Borradori, A-M Van Tuyll van Serooskerken, S Abraham, et al.
Differentiation; Research in Biological Diversity
|
August 1, 1993
Expression patterns of loricrin in various species and tissues
D Hohl, B Ruf Olano, P A de Viragh, et al.
Supportive Care in Cancer : Official Journal of the Multinational Association of Supportive Care in Cancer
|
August 26, 2016
Exploring the role of physician communication about adjuvant endocrine therapy among breast cancer patients on active treatment: a qualitative analysis
Albert J Farias, India J Ornelas, Sarah D Hohl, et al.
Experimental Dermatology
|
August 10, 1999
Hair shaft defects visualized after detergent extraction
R H Rice, V J Wong, M L Williams, et al.
Preventive Medicine Reports
|
July 22, 2022
Multi-component interventions and change in screening rates in primary care clinics in the Colorectal Cancer Control Program
Krishna P Sharma, Amy DeGroff, Sarah D Hohl, et al.
The British Journal of Dermatology
|
August 21, 2013
Identification of the first nonsense CDSN mutation with expression of a truncated protein causing peeling skin syndrome type B
A Mallet, M Kypriotou, K George, et al.
Progress in Community Health Partnerships : Research, Education, and Action
|
June 2, 2017
Engaging Study Participants in Research Dissemination at a Center for Population Health and Health Disparities
Sarah Knerr, Sarah D Hohl, Yamile Molina, et al.
The Journal of Investigative Dermatology
|
April 14, 1999
A novel substitution in keratin 10 in epidermolytic hyperkeratosis
M J Arin, M A Longley, I Anton-Lamprecht, et al.
Nature Genetics
|
August 1, 1994
Mutations in the rod domain of keratin 2e in patients with ichthyosis bullosa of Siemens
J A Rothnagel, H Traupe, S Wojcik, et al.
Page
of 15