Results 111 to 120 of about 6,707,637 (199)

Novel mutation in PTCH1 gene in a patient with basal cell nevus syndrome and uterus bicornis. [PDF]

open access: yesAn Bras Dermatol, 2019
Miyashiro D   +3 more
europepmc   +1 more source

A novel PTCH1 mutation in basal cell nevus syndrome with rare craniofacial features. [PDF]

open access: yesHum Genome Var, 2019
Murata Y   +13 more
europepmc   +1 more source

Odontogenic keratocysts are an important clue for diagnosing basal cell nevus syndrome

open access: yes
Basal cell nevus syndrome (BCNS) is an autosomal dominant skin disorder characterized by multiple basal cell nevi. Patients with BCNS tend to develop basal cell carcinoma (BCC) and frequently show skeletal abnormalities.
Kaibuchi-Ando, Kaori   +8 more
core  

Basal cell nevus syndrome (Gorlin-Goltz syndrome): genetic predisposition, clinical picture and treatment. [PDF]

open access: yesPostepy Dermatol Alergol, 2017
Witmanowski H   +4 more
europepmc   +1 more source

Sonic hedgehog signaling in Basal cell nevus syndrome. [PDF]

open access: yesCancer Res, 2014
Athar M   +4 more
europepmc   +1 more source

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