Coinheritance of naevoid basal cell carcinoma syndrome and neurofibromatosis type 1 associated with an exceptional spectrum of tumours
Br J Dermatol
.
2020 Dec;183(6):1108-1110.
doi: 10.1111/bjd.19324.
Epub 2020 Aug 2.
Authors
S J Ghadiri
1
,
P Brennan
2
,
E Calonje
3
,
A J Carmichael
1
,
N Rajan
4
5
Affiliations
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.
PMID:
32562549
DOI:
10.1111/bjd.19324
No abstract available
Publication types
Letter
Research Support, Non-U.S. Gov't
MeSH terms
Basal Cell Carcinoma*
Basal Cell Nevus Syndrome* / genetics
Humans
Neurofibromatosis 1* / complications
Skin Neoplasms* / genetics
Grants and funding
Newcastle NIHR Biomedical Research Centre
WT097163MA/WT_/Wellcome Trust/United Kingdom