Analysis of 133 meioses places the genes for nevoid basal cell carcinoma (Gorlin) syndrome and Fanconi anemia group C in a 2.6- cM interval and contributes to the fine map of 9q22.3

Tools

Item Type:	Article
Title:	Analysis of 133 meioses places the genes for nevoid basal cell carcinoma (Gorlin) syndrome and Fanconi anemia group C in a 2.6- cM interval and contributes to the fine map of 9q22.3
Creators Name:	Farndon, P.A., Morris, D.J., Hardy, C., McConville, C.M., Weissenbach, J., Kilpatrick, M.W. and Reis, A.
Source:	Genomics
ISSN:	0888-7543
Publisher:	Academic Press
Volume:	23
Page Range:	486-489
Date:	1 January 1994
PubMed:	View item in PubMed

Repository Staff Only: item control page