Coinheritance of naevoid basal cell carcinoma syndrome and neurofibromatosis type 1 associated with an exceptional spectrum of tumours-Reference-Cited by-同舟云学术

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Coinheritance of naevoid basal cell carcinoma syndrome and neurofibromatosis type 1 associated with an exceptional spectrum of tumours

Published:2020-08-02 Issue:6 Volume:183 Page:1108-1110
ISSN:0007-0963
Container-title:British Journal of Dermatology
language:en
Short-container-title:Br. J. Dermatol.

Author:

Ghadiri S.J.¹,Brennan P.²,Calonje E.³,Carmichael A.J.¹,Rajan N.⁴⁵^ORCID

Affiliation:

1. Department of Dermatology James Cook University Hospital Middlesbrough TS4 3BW UK

2. Clinical Genetics James Cook University Hospital Middlesbrough TS4 3BW UK

3. Department of Dermatopathology St John’s Institute of Dermatology St Thomas’ Hospital London SE1 7EH UK

4. Department of Dermatology Royal Victoria Infirmary Newcastle upon Tyne NE1 4LP UK

5. Translational and Clinical Research Institute Newcastle University Newcastle upon Tyne NE1 3BZ UK

Funder

Wellcome

Publisher

Wiley

Subject

Dermatology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/bjd.19324

Reference7 articles.

1. Gorlin's syndrome and von Recklinghausen's disease occurring in one family

2. Complications of the naevoid basal cell carcinoma syndrome: results of a population based study.

3. Neurofibromatosis type 1-associated tumours: Their somatic mutational spectrum and pathogenesis

4. Glomus tumors in individuals with neurofibromatosis type 1

5. NF1-Associated Gastrointestinal Stromal Tumors Have Unique Clinical, Phenotypic, and Genotypic Characteristics

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