Whole-exome sequencing of nevoid basal cell carcinoma syndrome families and review of Human Gene Mutation Database PTCH1 mutation data-Reference-Cited by-同舟云学术

Whole-exome sequencing of nevoid basal cell carcinoma syndrome families and review of Human Gene Mutation Database PTCH1 mutation data

Published:2018-11 Issue:6 Volume:6 Page:1168-1180
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Gianferante D. Matthew¹^ORCID,Rotunno Melissa²,Dean Michael¹,Zhou Weiyin³,Hicks Belynda D.¹³,Wyatt Kathleen³,Jones Kristine¹³,Wang Mingyi³,Zhu Bin³,Goldstein Alisa M.¹,Mirabello Lisa¹

Affiliation:

1. Division of Cancer Epidemiology and Genetics; National Cancer Institute, National Institutes of Health; Bethesda Maryland

2. Division of Cancer Control and Population Science; National Cancer Institute, National Institutes of Health; Bethesda Maryland

3. Cancer Genomics Research Laboratory, Leidos Biomedical Research; Frederick National Laboratory for Cancer Research; Frederick Maryland

Funder

Intramural Research Program of the Division of Cancer Epidemiology and Genetics of the National Cancer Institute

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/mgg3.498/fullpdf

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3. Spectrum of PTCH1 mutations in French patients with Gorlin syndrome;Boutet;The Journal of Investigative Dermatology,2003

4. Consensus statement from the first international colloquium on basal cell nevus syndrome (BCNS);Bree;American Journal of Medical Genetics. Part A,2011

5. Nevoid basal cell carcinoma syndrome (Gorlin Syndrome);Bresler;Head Neck Pathol,2016

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