Full text
PDFSelected References
These references are in PubMed. This may not be the complete list of references from this article.
- Anderson D. E., Taylor W. B., Falls H. F., Davidson R. T. The nevoid basal cell carcinoma syndrome. Am J Hum Genet. 1967 Jan;19(1):12–22. [PMC free article] [PubMed] [Google Scholar]
- Bale S. J., Amos C. I., Parry D. M., Bale A. E. Relationship between head circumference and height in normal adults and in the nevoid basal cell carcinoma syndrome and neurofibromatosis type I. Am J Med Genet. 1991 Aug 1;40(2):206–210. doi: 10.1002/ajmg.1320400217. [DOI] [PubMed] [Google Scholar]
- Crosby J. L., Varnum D. S., Nadeau J. H. Two-hit model for sporadic congenital anomalies in mice with the disorganization mutation. Am J Hum Genet. 1993 May;52(5):866–874. [PMC free article] [PubMed] [Google Scholar]
- Farndon P. A., Del Mastro R. G., Evans D. G., Kilpatrick M. W. Location of gene for Gorlin syndrome. Lancet. 1992 Mar 7;339(8793):581–582. doi: 10.1016/0140-6736(92)90868-4. [DOI] [PubMed] [Google Scholar]
- Fraser F. C. The William Allan Memorial Award Address: evolution of a palatable multifactorial threshold model. Am J Hum Genet. 1980 Nov;32(6):796–813. [PMC free article] [PubMed] [Google Scholar]
- Gailani M. R., Bale S. J., Leffell D. J., DiGiovanna J. J., Peck G. L., Poliak S., Drum M. A., Pastakia B., McBride O. W., Kase R. Developmental defects in Gorlin syndrome related to a putative tumor suppressor gene on chromosome 9. Cell. 1992 Apr 3;69(1):111–117. doi: 10.1016/0092-8674(92)90122-s. [DOI] [PubMed] [Google Scholar]
- Gailani M. R., Ståhle-Bäckdahl M., Leffell D. J., Glynn M., Zaphiropoulos P. G., Pressman C., Undén A. B., Dean M., Brash D. E., Bale A. E. The role of the human homologue of Drosophila patched in sporadic basal cell carcinomas. Nat Genet. 1996 Sep;14(1):78–81. doi: 10.1038/ng0996-78. [DOI] [PubMed] [Google Scholar]
- Goldstein A. M., Pastakia B., DiGiovanna J. J., Poliak S., Santucci S., Kase R., Bale A. E., Bale S. J. Clinical findings in two African-American families with the nevoid basal cell carcinoma syndrome (NBCC). Am J Med Genet. 1994 Apr 15;50(3):272–281. doi: 10.1002/ajmg.1320500311. [DOI] [PubMed] [Google Scholar]
- Gorlin R. J. Nevoid basal cell carcinoma syndrome. Dermatol Clin. 1995 Jan;13(1):113–125. [PubMed] [Google Scholar]
- Hahn H., Wicking C., Zaphiropoulous P. G., Gailani M. R., Shanley S., Chidambaram A., Vorechovsky I., Holmberg E., Unden A. B., Gillies S. Mutations of the human homolog of Drosophila patched in the nevoid basal cell carcinoma syndrome. Cell. 1996 Jun 14;85(6):841–851. doi: 10.1016/s0092-8674(00)81268-4. [DOI] [PubMed] [Google Scholar]
- Knudson A. G., Jr Mutation and cancer: statistical study of retinoblastoma. Proc Natl Acad Sci U S A. 1971 Apr;68(4):820–823. doi: 10.1073/pnas.68.4.820. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Levanat S., Gorlin R. J., Fallet S., Johnson D. R., Fantasia J. E., Bale A. E. A two-hit model for developmental defects in Gorlin syndrome. Nat Genet. 1996 Jan;12(1):85–87. doi: 10.1038/ng0196-85. [DOI] [PubMed] [Google Scholar]
- Motzny C. K., Holmgren R. The Drosophila cubitus interruptus protein and its role in the wingless and hedgehog signal transduction pathways. Mech Dev. 1995 Jul;52(1):137–150. doi: 10.1016/0925-4773(95)00397-j. [DOI] [PubMed] [Google Scholar]
- Pennisi E. Gene linked to commonest cancer. Science. 1996 Jun 14;272(5268):1583–1584. doi: 10.1126/science.272.5268.1583. [DOI] [PubMed] [Google Scholar]
- Phillips R. G., Roberts I. J., Ingham P. W., Whittle J. R. The Drosophila segment polarity gene patched is involved in a position-signalling mechanism in imaginal discs. Development. 1990 Sep;110(1):105–114. doi: 10.1242/dev.110.1.105. [DOI] [PubMed] [Google Scholar]
- Reis A., Küster W., Linss G., Gebel E., Hamm H., Fuhrmann W., Wolff G., Groth W., Gustafson G., Kuklik M. Localisation of gene for the naevoid basal-cell carcinoma syndrome. Lancet. 1992 Mar 7;339(8793):617–617. doi: 10.1016/0140-6736(92)90903-g. [DOI] [PubMed] [Google Scholar]
- Shimkets R., Gailani M. R., Siu V. M., Yang-Feng T., Pressman C. L., Levanat S., Goldstein A., Dean M., Bale A. E. Molecular analysis of chromosome 9q deletions in two Gorlin syndrome patients. Am J Hum Genet. 1996 Aug;59(2):417–422. [PMC free article] [PubMed] [Google Scholar]
- Strong L. C. Genetic and environmental interactions. Cancer. 1977 Oct;40(4 Suppl):1861–1866. doi: 10.1002/1097-0142(197710)40:4+<1861::aid-cncr2820400815>3.0.co;2-9. [DOI] [PubMed] [Google Scholar]
- Xu T., Wang W., Zhang S., Stewart R. A., Yu W. Identifying tumor suppressors in genetic mosaics: the Drosophila lats gene encodes a putative protein kinase. Development. 1995 Apr;121(4):1053–1063. doi: 10.1242/dev.121.4.1053. [DOI] [PubMed] [Google Scholar]
- Ziegler A., Leffell D. J., Kunala S., Sharma H. W., Gailani M., Simon J. A., Halperin A. J., Baden H. P., Shapiro P. E., Bale A. E. Mutation hotspots due to sunlight in the p53 gene of nonmelanoma skin cancers. Proc Natl Acad Sci U S A. 1993 May 1;90(9):4216–4220. doi: 10.1073/pnas.90.9.4216. [DOI] [PMC free article] [PubMed] [Google Scholar]