Results 171 to 180 of about 5,711 (254)

Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex

open access: bronze, 2018
M. T. Romano   +21 more
openalex   +1 more source

A Child with Hallermann-Streiff Syndrome; as an Infrequent Cause of Hypotrichosis and Cataract

open access: bronze, 2019
Sultan Kaba   +6 more
openalex   +1 more source

Dermatology [PDF]

open access: yes, 2013
三澤 恵   +9 more
core   +2 more sources

Genetic profiling and diagnostic strategies for patients with ectodermal dysplasias in Korea. [PDF]

open access: yesOrphanet J Rare Dis
Kim MJ   +7 more
europepmc   +1 more source

Hair Evaluation in Orthodontic Patients with Oligodontia. [PDF]

open access: yesDiagnostics (Basel)
Zadurska M   +7 more
europepmc   +1 more source

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