Results 241 to 250 of about 7,293 (261)

Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis

Nature Genetics, 2009
Yaran Wen, Sven Cichon, Markus M Nöthen
exaly  

Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing

Journal of Investigative Dermatology, 2009
Hans Christian Hennies
exaly  

Oculomandibulodyscephaly with hypotrichosis

The Journal of Pediatrics, 1967
openaire   +1 more source

Congenital hypotrichosis in two dogs

Journal of the American Veterinary Medical Association, 1984
openaire   +2 more sources

A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis

Journal of Investigative Dermatology, 2012
Muhammad Farooq, Asuka Inoue, Manabu Ohyama   +2 more
exaly  

A mutation in the lipase H (LIPH) gene underlie autosomal recessive hypotrichosis

Human Genetics, 2007
Ghazanfar Ali, Wasim Ahmad
exaly  

A Deletion in FOXN1 Is Associated with a Syndrome Characterized by Congenital Hypotrichosis and Short Life Expectancy in Birman Cats

PLoS ONE, 2015
Marie Abitbol, Laurent Tiret
exaly  

Mutations in the Desmoglein 4 Gene Are Associated with Monilethrix-like Congenital Hypotrichosis

Journal of Investigative Dermatology, 2006
Yutaka Shimomura
exaly  

Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions

Journal of Investigative Dermatology, 2006
Hisham Bazzi
exaly  

Oculomandibulodyscephaly with hypotrichosis

2004
openaire   +1 more source