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 (Q28306269)
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Current Data About 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
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(P577) Thursday, September 15, 1994

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(P1476) "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" (language: en)

(P2093) P A Farndon
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D J Morris
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C Hardy
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C M McConville
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M W Kilpatrick
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A Reis
(P1545) 7

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External Links
(P356) 10.1006/GENO.1994.1528
(P698) 7835901