Cutaneous hyperpigmentation and familial gastrointestinal stromal tumour associated with KIT mutation. [electronic resource]
Producer: 20200106Description: 418-421 p. digitalISSN:- 1365-2230
- Child
- Gastrointestinal Stromal Tumors -- diagnosis
- Germ-Line Mutation -- genetics
- Humans
- Hyperpigmentation -- diagnosis
- Lentigo -- pathology
- Male
- Mass Screening -- standards
- Mutation
- Proto-Oncogene Proteins c-kit -- genetics
- Skin Diseases, Genetic -- diagnosis
- Urticaria Pigmentosa -- pathology
- Vitiligo -- pathology
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Publication Type: Case Reports; Journal Article
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