The 'Sins' of the fathers: Self-healing squamous epithelioma in scotland

Journal of Cutaneous Medicine and Surgery

Volumn 3, Issue 4, 1999, Pages 207-210

  Bale, Sherri J ^a,b  

^a NATIONAL INSTITUTES OF HEALTH   (United States)

^b NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CHROMOSOME 9Q; FOUNDER EFFECT; GENE MAPPING; GENODERMATOSIS; HAPLOTYPE; HEALING; HUMAN; PRIORITY JOURNAL; SQUAMOUS CELL CARCINOMA; UNITED KINGDOM;

EID: 0032930572     PISSN: 12034754     EISSN: None     Source Type: Journal    
DOI: 10.1177/120347549900300411     Document Type: Article

References (8)

1. Ferguson Smith J. A case of multiple primary squamous-celled carcinomata of the skin in a young man, with spontaneous healing. Br J Dermatol 1934; 46:267-272.
2. Ferguson-Smith MA, Wallace DC, James ZH, Renwick JH. Multiple self-healing squamous epithelioma. Birth Defects Orig Art Ser 1971; 7:157-163.
3. Sybert VP. Genetic skin disorders. Oxford, UK: Oxford University Press, 1997:511-513.
4. Goudie DR, Yuille MA, Leversha MA, et al. Multiple self-healing squamous epitheliomata (ESS1) mapped to chromosome 9q22-q31 in families with common ancestry. Nat Genet 1993; 3:165-169.
5. King RC, Stansfield WC. A dictionary of genetics. Oxford, UK: Oxford University Press, 1997:130.
6. Bale SJ. When genetics gets under your skin. J Cutan Med Surg 1996; 1:97-100.
7. Richards FB, Goudie DR, Cooper WN, et al. Mapping the multiple self-healing squamous epithelioma (MSSE) gene and investigation of xeroderma pigmentosum group A (XPA) and PATCHED (PTCH) as candidate genes. Hum Genet 1997; 101:317-322.
8. Gailani MR, Bale SJ, Leffell DJ, et al. Developmental defects in Gorlin syndrome related to a putative tumor suppressor gene on chromosome 9. Cell 1992; 69:111-117.