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

Author:

Gianferante D. Matthew1ORCID,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

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