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Article

Frameshift mutation in the PTCH2 gene can cause nevoid basal cell carcinoma syndrome

11 Mar 2013

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 23479190
DOI: 10.1007/s10689-013-9623-1

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Frameshift mutation in the PTCH2 gene can cause nevoid basal cell carcinoma syndromePMID 23479190Read ↗

A novel PTCH1 mutation in a patient of nevoid basal cell carcinoma syndrome.Semantic proximity Read ↗

Novel mutation in PTCH1 gene in a patient with basal cell nevus syndrome and uterus bicornis.Semantic proximity Read ↗

A healthy individual with a homozygous PTCH2 frameshift variant: Are variants of PTCH2 associated with nevoid basal cell carcinoma syndrome?Semantic proximity Read ↗

Germline mutations of the PTCH gene in Japanese patients with nevoid basal cell carcinoma syndrome.Semantic proximity Read ↗

Novel PTCH1 Gene Mutation in Nevoid Basal Cell Carcinoma Syndrome.Semantic proximity Read ↗

Nevoid basal cell carcinoma syndrome with cleft lip and palate associated with the novel PTCH gene mutations.Semantic proximity Read ↗

PTCH mutations and deletions in patients with typical nevoid basal cell carcinoma syndrome and in patients with a suspected genetic predisposition to basal cell carcinoma: a French study.Semantic proximity Read ↗

PTCH mutations: distribution and analyses.Semantic proximity Read ↗

Nevoid basal cell carcinoma syndrome caused by splicing mutations in the PTCH1 gene.Semantic proximity Read ↗

A novel mutation of the PTCH1 gene activates the Shh/Gli signaling pathway in a Chinese family with nevoid basal cell carcinoma syndrome.Semantic proximity Read ↗

Somatic mosaicism containing double mutations in PTCH1 revealed by generation of induced pluripotent stem cells from nevoid basal cell carcinoma syndrome.Semantic proximity Read ↗

Mutations of PTCH1 gene in two pedigrees with bifid rib-basal cell nevus-jaw cyst syndrome.Semantic proximity Read ↗

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