Results 131 to 140 of about 5,312 (215)

A Recurrent Intragenic Deletion Mutation in DSG4 Gene in Three Pakistani Families with Autosomal Recessive Hypotrichosis [PDF]

, 2004
Muhammad Rafiq, Muhammad Ansar, Saqib Mahmood, Sayedul Haque, Muhammad Faiyaz‐Ul‐Haque, Suzanne M. Leal, Wasim Ahmad   +6 more
openalex   +1 more source

Ichthyosis-hypotrichosis syndrome [PDF]

, 2020
openaire   +1 more source

Expanding the Cutaneous Spectrum of Nicolaides‑Baraitser Syndrome: Eczema and Generalized Hair Loss. [PDF]

Cureus
Moreno BA, Torres K, Duarte A.
europepmc   +1 more source

Correction: Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report. [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

Keratoderma-hypotrichosis-leukonychia Totalis Syndrome: A New Case Report of an Exceptional Entity. [PDF]

Acta Derm Venereol
Gutiérrez-Cerrajero C, Gestoso-Uzal N, Ortiz-Cabrera NV, González-Sarmiento R, Hernández-Martín Á.   +4 more
europepmc   +1 more source

Topical minoxidil effectiveness in enhancing facial aesthetics: A systematic review and meta-analysis. [PDF]

J Family Med Prim Care
Almutairi AG, Shadid A, AlAkrash L.
europepmc   +1 more source

Hereditary Hypotrichosis in the Rat (Mus Norvegicus)

, 1940
E. Roberts, J.H. Quisenberry, Langer Thomas   +2 more
openalex   +1 more source

Multistage orthodontic-implantology-prosthetic treatment of a patient diagnosed with hypohidrosis ectodermal dysplasia syndrome with EDAR mutation: a case report. [PDF]

BMC Oral Health
Huang C, Yan Y, Algahefi A, Al-Tayar B, Zheng B.   +4 more
europepmc   +1 more source

Hypotrichosis simplex type 7: A rare cause of non-syndromic woolly hair

Priyansh Gupta, Priyanka Sangwan, Vishal Thakur, Biswanath Behera   +3 more
openalex   +1 more source

A case study of a novel homozygous EDAR splice site variant in hypohidrotic ectodermal dysplasia with tooth agenesis: molecular dynamics insights. [PDF]

BMC Med Genomics
Nejati P, Khosravi T, Lorestani S, Oladnabi M.   +3 more
europepmc   +1 more source