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Clinical and Experimental Dermatology
|
December 2, 2015
Isotretinoin treatment of autosomal recessive congenital ichthyosis complicated by coexisting dysferlinopathy
J Mashiah, A Harel, O Bitterman, et al.
Clinical and Experimental Dermatology
|
October 13, 2016
A novel homozygous deletion in EXPH5 causes a skin fragility phenotype
N Malchin, O Sarig, M Grafi-Cohen, et al.
The British Journal of Dermatology
|
November 29, 2019
Symptomatic mucosal involvement in pachyonychia congenita: challenges in infants and young children
I Goldberg, J Mashiah, A Kutz, et al.
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of 2
Search research articles
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Showing results (11-20 of 13) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 13 results.
Clinical and Experimental Dermatology
|
December 2, 2015
Isotretinoin treatment of autosomal recessive congenital ichthyosis complicated by coexisting dysferlinopathy
J Mashiah, A Harel, O Bitterman, et al.
Clinical and Experimental Dermatology
|
October 13, 2016
A novel homozygous deletion in EXPH5 causes a skin fragility phenotype
N Malchin, O Sarig, M Grafi-Cohen, et al.
The British Journal of Dermatology
|
November 29, 2019
Symptomatic mucosal involvement in pachyonychia congenita: challenges in infants and young children
I Goldberg, J Mashiah, A Kutz, et al.
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of 2