Author:
Altaraihi M.,Wadt K.,Ek J.,Gerdes A. M.,Ostergaard E.
Publisher
Springer Science and Business Media LLC
Subject
Genetics,Molecular Biology,Biochemistry
Reference16 articles.
1. Smyth, I. et al. Isolation and characterization of human patched 2 (PTCH2), a putative tumour suppressor gene inbasal cell carcinoma and medulloblastoma on chromosome 1p32. Hum. Mol. Genet. 8, 291–7 (1999).
2. Evans, D. G. et al. Complications of the naevoid basal cell carcinoma syndrome: results of a population based study. J. Med. Genet. 30, 460–4 (1993).
3. Evans D. G., Farndon P. A. Nevoid Basal Cell Carcinoma Syndrome. (eds Adam M. P., Ardinger H. H., Pagon R. A., Wallace S. E., Bean L. J. H., Stephens K.) (GeneReviews((R)), Seattle (WA), 1993).
4. Bare, J. W., Lebo, R. V. & Epstein, E. H. Jr. Loss of heterozygosity at chromosome 1q22 in basal cell carcinomas and exclusion of the basal cell nevus syndrome gene from this site. Cancer Res. 52, 1494–8 (1992).
5. Bialer, M. G., Gailani, M. R., McLaughlin, J. A., Petrikovsky, B. & Bale, A. E. Prenatal diagnosis of Gorlin syndrome. Lancet 344, 477 (1994).
Cited by
13 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献