✦ LIBER ✦

Unique features of PTCH1 mutation spectrum in Chinese sporadic basal cell carcinoma

✍ Scribed by Y.S. Huang; D.F. Bu; X.Y. Li; Z.H. Ma; Y. Yang; Z.M. Lin; F.M. Lu; P. Tu; H. Li

Book ID: 111099016
Publisher: John Wiley and Sons
Year: 2012
Tongue: English
Weight: 333 KB
Volume: 27
Category: Article
ISSN: 0926-9959
DOI: 10.1111/j.1468-3083.2012.04453.x

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

PTCH germline mutations in Chinese nevoi

PTCH germline mutations in Chinese nevoid basal cell carcinoma syndrome patients

✍ T-J Li; J-W Yuan; X-M Gu; L-S Sun; H-S Zhao 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 247 KB

Mutational analysis of the SHH and PTCH

Mutational analysis of the SHH and PTCH genes in sporadic basal cell carcinomas

✍ Reifenberger, J.; Wolter, M.; Schulte, K.W.; Megahed, M.; Ruzicka, T.; Reifenber 📂 Article 📅 1998 🏛 Elsevier Science 🌐 English ⚖ 183 KB

UV-specific p53 and PTCH mutations in sp

UV-specific p53 and PTCH mutations in sporadic basal cell carcinoma of sun-exposed skin

✍ Désirée Ratner; Monica Peacocke; Hong Zhang; Xiao Li Ping a; Hui C. Tsou 📂 Article 📅 2001 🏛 Elsevier Science 🌐 English ⚖ 383 KB

Somatic mutations in the PTCH, SMOH, SUF

Somatic mutations in the PTCH, SMOH, SUFUH and TP53 genes in sporadic basal cell carcinomas

✍ J. Reifenberger; M. Wolter; C. B. Knobbe; B. Köhler; A. Schönicke; C. Scharwächt 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 195 KB

A novel PTCH1 mutation in a patient of n

A novel PTCH1 mutation in a patient of nevoid basal cell carcinoma syndrome

✍ Honma, Masaru; Ohishi, Yasushi; Uehara, Jiro; Ibe, Masaki; Kinouchi, Motoshi; Is 📂 Article 📅 2008 🏛 Elsevier Science 🌐 English ⚖ 446 KB

Spectrum of PTCH mutations in Italian ne

Spectrum of PTCH mutations in Italian nevoid basal cell-carcinoma syndrome patients: Identification of thirteen novel alleles

✍ Maria Savino; Maria d'Apolito; Vincenza Formica; Filomena Baorda; Francesca Mari 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 57 KB 👁 1 views

The nevoid basal cell carcinoma syndrome (NBCCS) is an autosomal dominant genetic disease characterized by numerous basal cell carcinomas, odontogenic keratocysts of the jaws, palmar and plantal pits, skeletal abnormalities, and calcification of the falx cerebri. The gene responsible for this syndro