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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

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

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