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Foreword by Robert J Gorlin
Cancerassociated Genodermatoses and Internal Manifestations
Cutaneous Signs of Cancerassociated Genodermatoses
9 other sections not shown
abnormalities adenocarcinoma adenoma anemia antibody antigens Arch areas associated ataxia telangiectasia atypical autosomal dominant basal cell carcinoma biopsies cancer-associated genodermatoses chromosomal chronic classical XP clinical colon congenital cutaneous cysts damage defect deficiency Derm Dermatol dermis develop diagnosis disease disorder DNA repair epidermal excision repair FAMMM FAMMM syndrome fibroblasts Figure Gardner's syndrome gastrointestinal gene genetic hemochromatosis hereditary heterozygous histologic immune immunodeficiency immunoglobulin immunologic increased infections inherited intestinal involved irradiation keratoacanthoma lait spots lesions lymphocytes Lymphoid Lynch malignant melanoma manifestations melanocytes metastatic Mitogens moles multiple neoplasms neurocristic neurofibromas neurofibromatosis neuroma nevi nevus normal occur papillary dermis Peutz-Jeghers syndrome phenotype pigmented plasma polyposis polyps present primary proband PUVA pyrimidine dimers Reduced or absent reported response sarcoma sebaceous sebaceous adenomas serum SqCC squamous cell carcinoma thyroid tion tissue tuberous sclerosis tumors usually Wiskott-Aldrich syndrome xeroderma pigmentosum XP cells XP patients XP variant