Genetic mapping of the FACC gene and linkage analysis in Fanconi anaemia families.

Fanconi anaemia is an autosomal recessive disorder associated with increased chromosome breakage and progressive bone marrow failure. The gene for complementation group C (FACC) has been cloned and mapped to chromosome 9q22.3, but neither its genetic location nor the proportion of patients belonging...

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Библиографические подробности
Главные авторы: Gibson, R A, Ford, D, Jansen, S, Savoia, A, Havenga, C, Milner, R D, de Ravel, T J, Cohn, R J, Ball, S E, Roberts, I
Формат: Artigo
Язык:Inglês
Опубликовано: 1994
Предметы:
Research Article
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC1016661/
https://ncbi.nlm.nih.gov/pubmed/7853372
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