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Nucleic Acids Research
|
February 13, 2008
Small RNAs encoded within genetic islands of Salmonella typhimurium show host-induced expression and role in virulence
Gilly Padalon-Brauch, Ruth Hershberg, Maya Elgrably-Weiss, et al.
The Journal of Investigative Dermatology
|
April 23, 2013
Semidominant inheritance in epidermolytic ichthyosis
Janna Nousbeck, Gilly Padalon-Brauch, Dana Fuchs-Telem, et al.
The Journal of Investigative Dermatology
|
July 27, 2012
Digenic inheritance in epidermolysis bullosa simplex
Gilly Padalon-Brauch, Dani Ben Amitai, Dan Vodo, et al.
Experimental Dermatology
|
March 27, 2013
The sound of silence: autosomal recessive congenital ichthyosis caused by a synonymous mutation in ABCA12
Tomer Goldsmith, Dana Fuchs-Telem, Shirli Israeli, et al.
American Journal of Human Genetics
|
July 31, 2012
Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis syndrome is caused by a POC1A mutation
Ofer Sarig, Sagi Nahum, Debora Rapaport, et al.
Nature Genetics
|
November 8, 2016
Stabilizing mutations of KLHL24 ubiquitin ligase cause loss of keratin 14 and human skin fragility
Zhimiao Lin, Shuo Li, Cheng Feng, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 6) with videos related to
Sort By:
Page
of 1
Nucleic Acids Research
|
February 13, 2008
Small RNAs encoded within genetic islands of Salmonella typhimurium show host-induced expression and role in virulence
Gilly Padalon-Brauch, Ruth Hershberg, Maya Elgrably-Weiss, et al.
The Journal of Investigative Dermatology
|
April 23, 2013
Semidominant inheritance in epidermolytic ichthyosis
Janna Nousbeck, Gilly Padalon-Brauch, Dana Fuchs-Telem, et al.
The Journal of Investigative Dermatology
|
July 27, 2012
Digenic inheritance in epidermolysis bullosa simplex
Gilly Padalon-Brauch, Dani Ben Amitai, Dan Vodo, et al.
Experimental Dermatology
|
March 27, 2013
The sound of silence: autosomal recessive congenital ichthyosis caused by a synonymous mutation in ABCA12
Tomer Goldsmith, Dana Fuchs-Telem, Shirli Israeli, et al.
American Journal of Human Genetics
|
July 31, 2012
Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis syndrome is caused by a POC1A mutation
Ofer Sarig, Sagi Nahum, Debora Rapaport, et al.
Nature Genetics
|
November 8, 2016
Stabilizing mutations of KLHL24 ubiquitin ligase cause loss of keratin 14 and human skin fragility
Zhimiao Lin, Shuo Li, Cheng Feng, et al.
Page
of 1