Results 141 to 150 of about 1,227,280 (190)

A novel homozygous intronic variant in CDT1 that alters splicing causes Meier-Gorlin syndrome, and a review of published mutations and growth hormone treatments. [PDF]

Orphanet J Rare Dis
Li Q, Wu Y, Meng F, Li Z, Zhan D, Luo X.
europepmc   +1 more source

Further Expanding the Mutational Spectrum of Gorlin Syndrome in Three Unrelated Families. [PDF]

Mol Syndromol
Kolkiran A, Şimşek-Kiper PÖ, Topaloğlu Yasan G, Karaosmanoğlu B, Taşkıran E, Utine GE, Tüz HH, Boduroğlu K.   +7 more
europepmc   +1 more source

Pediatric odontogenic keratocyst and early diagnosis of Gorlin syndrome: Clinicopathological aids. [PDF]

Saudi Dent J
Bello IO.
europepmc   +1 more source

Use of Anti-PD1 Blockade After Hedgehog Inhibitors or as First-Line Therapy for Gorlin Syndrome.

JAMA Dermatol
Reschke R, Richter J, Enk AH, Hassel JC.
europepmc   +1 more source

[Gorlin syndrome].

Vestnik dermatologii i venerologii, 1983
A A, Kalamkarian, V V, Kapkin, I I, Bogatyreva, A M, Vavilov, A V, Mikhaĭlovskiĭ   +4 more
openaire   +1 more source

[Gorlin's syndrome].

Revista brasileira de odontologia, 1969
openaire   +1 more source

[Gorlin syndrome].

Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke, 1987
A, Helseth, E A, Mylius
openaire   +1 more source

Location of Gene for Gorlin Syndrome

Lancet, The, 1992
The Gorlin (naevoid-basal-cell-carcinoma) syndrome is an autosomal dominant disorder characterised by multiple naevoid basal-cell carcinomas, recurrent odontogenic keratocysts, skeletal anomalies, intracranial calcification, and developmental ...
Gareth Evans, P A Farndon
exaly   +7 more sources