Results 131 to 140 of about 8,285 (255)

A Novel Mutation in the OFD1 Gene in a Family with Oral-Facial-Digital Syndrome Type 1: A Case Report. [PDF]

, 2016
Oral-facial-digital syndrome as heterogeneous developmental conditions is characterized by abnormalities in the oral cavity, facial features and digits.
Baple, EL, Chioza, BA, Crosby, AH, Dehghan Tezerjani, M, Dehghani, M, Ghadimi, H, Kalantar, SM, Maroofian, R, Nori-Shadkam, M, Vahidi Mehrjardi, MY, Zamaninejad, S   +10 more
core  

A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis [PDF]

, 2018
Chen, Fuyin, Li, Chengrang, Li, Ming, Ni, Cheng, Sandilands, Aileen, Yao, Zhirong, Yu, Xia, Zhang, Guolong, Zhang, Jia, Zheng, Luyao   +9 more
core   +2 more sources

Topobiology of Human Pigmentation: P-Cadherin Selectively Stimulates Hair Follicle Melanogenesis [PDF]

, 2017
Bíró, Tamás, Kloepper, Jennifer E., Paus, Ralf, Samuelov, Liat, Singh, Suman K., Sprecher, Eli, Sugawara, Koji, Tobin, Desmund J., Tsuruta, Daisuke   +8 more
core   +1 more source

Bimatoprost in the treatment of eyelash hypotrichosis

Clinical Ophthalmology, 2010
Simon K LawJules Stein Eye Institute, University of California, Los Angeles, California, USAAbstract: Eyelashes hypotrichosis is a condition indicated by an inadequate amount of eyelashes.
Simon K Law
doaj  

Hypotrichosis simplex [PDF]

, 2020
openaire   +1 more source

Loss-of-function variants in C3ORF52 result in localized autosomal recessive hypotrichosis

Genetics in Medicine, 2020
L. Malki, O. Sarig, N. Cesarato, J. Mohamad, T. Canter, S. Assaf, M. Pavlovsky, D. Vodo, Y. Anis, O. Bihari, K. Malovitski, A. Gat, H. Thiele, B. E. White, L. Samuelov, A. Nanda, A. Paller, R. Betz, E. Sprecher   +18 more
semanticscholar   +1 more source

Autosomal recessive woolly hair syndrome: a series of eight patients in an Indian population. [PDF]

Skin Health Dis
Somani V, Somani A, Annabathula A.
europepmc   +1 more source

Ichthyosis-hypotrichosis syndrome [PDF]

, 2020
openaire   +1 more source

Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis. [PDF]

Front Med (Lausanne)
Xie Y, Luo S, Yang Y, Zou X, Lv S, Du M, Xu Y, Song X, Qi C, Li N, Yang D.   +10 more
europepmc   +1 more source

A classical variant of ectodermal dysplasia: a case report. [PDF]

Pan Afr Med J
Jawade S, Wankhede P, Sharma R, Munjewar P, More V.   +4 more
europepmc   +1 more source