Multiple Hereditary Infundibulocystic Basal Cell Carcinoma Syndrome Associated With a GermlineSUFUMutation-Reference-Cited by-同舟云学术

Multiple Hereditary Infundibulocystic Basal Cell Carcinoma Syndrome Associated With a GermlineSUFUMutation

Published:2016-03-01 Issue:3 Volume:152 Page:323
ISSN:2168-6068
Container-title:JAMA Dermatology
language:en
Short-container-title:JAMA Dermatol

Author:

Schulman Joshua M.¹,Oh Dennis H.²,Sanborn J. Zachary³,Pincus Laura¹,McCalmont Timothy H.¹,Cho Raymond J.⁴

Affiliation:

1. Department of Dermatology, University of California, San Francisco2Department of Pathology, University of California, San Francisco

2. Department of Dermatology, University of California, San Francisco3Dermatology Research Unit, San Francisco Veterans Affairs Medical Center, San Francisco, California

3. NantOmics, LLC, Santa Cruz, California

4. Department of Dermatology, University of California, San Francisco

Publisher

American Medical Association (AMA)

Subject

Dermatology

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1. Skin and Lacrimal Drainage System;Ocular Pathology;2025

2. Clinicopathological and molecular spectrum of patients with germline SUFU mutations: A case series;Journal of Cutaneous Pathology;2024-09-14

3. Mosaic SUFU mutation associated with a mild phenotype of multiple hereditary infundibulocystic basal cell carcinoma syndrome;The Journal of Dermatology;2024-08-19

4. Medulloblastoma and other neoplasms in patients with heterozygous germline SUFU variants: A scoping review;American Journal of Medical Genetics Part A;2024-01-28

5. Nonsense‐Mutation in SUFU ist mit multiplen infundibulozystischen Basalzellkarzinomen assoziiert;JDDG: Journal der Deutschen Dermatologischen Gesellschaft;2023-11