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Tom Rabinowitz

Showing results (11-20 of 14) with videos related to

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Molecular Vision|March 2, 2019
A novel intronic mutation of <i>PDE6B</i> is a major cause of autosomal recessive retinitis pigmentosa among Caucasus JewsYasmin Tatour, Jonathan Tamaiev, Shamaly Shamaly, et al.
The Journal of Investigative Dermatology|May 15, 2018
Filaggrin 2 Deficiency Results in Abnormal Cell-Cell Adhesion in the Cornified Cell Layers and Causes Peeling Skin Syndrome Type AJanan Mohamad, Ofer Sarig, Lisa M Godsel, et al.
The New England Journal of Medicine|February 15, 2019
Variant <i>PADI3</i> in Central Centrifugal Cicatricial AlopeciaLiron Malki, Ofer Sarig, Maria-Teresa Romano, et al.
Experimental Dermatology|March 31, 2021
Molecular epidemiology of non-syndromic autosomal recessive congenital ichthyosis in a Middle-Eastern populationJanan Mohamad, Liat Samuelov, Natalia Malchin, et al.
Pageof 2

Showing results (11-20 of 14) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 14 results.
Molecular Vision|March 2, 2019
A novel intronic mutation of <i>PDE6B</i> is a major cause of autosomal recessive retinitis pigmentosa among Caucasus JewsYasmin Tatour, Jonathan Tamaiev, Shamaly Shamaly, et al.
The Journal of Investigative Dermatology|May 15, 2018
Filaggrin 2 Deficiency Results in Abnormal Cell-Cell Adhesion in the Cornified Cell Layers and Causes Peeling Skin Syndrome Type AJanan Mohamad, Ofer Sarig, Lisa M Godsel, et al.
The New England Journal of Medicine|February 15, 2019
Variant <i>PADI3</i> in Central Centrifugal Cicatricial AlopeciaLiron Malki, Ofer Sarig, Maria-Teresa Romano, et al.
Experimental Dermatology|March 31, 2021
Molecular epidemiology of non-syndromic autosomal recessive congenital ichthyosis in a Middle-Eastern populationJanan Mohamad, Liat Samuelov, Natalia Malchin, et al.
Pageof 2