The genetic and molecular basis of Fanconi anemia
Author:
Publisher
Elsevier BV
Subject
Health, Toxicology and Mutagenesis,Genetics,Molecular Biology
Reference98 articles.
1. Familiäre infantile perniziosartige anämie (pernizioses blutbild und konstitution);Fanconi;Jahrb. Kinderh.,1927
2. Spontane chromosomenaberrationen bei familiärer panmyelopathie;Schroeder;Humangenetik,1964
3. Is Fanconi's anaemia defective in a process essential for the repair of DNA cross links?;Sasaki;Nature,1975
4. Susceptibility of Fanconi's anaemia fibroblasts to chromosome damage by carcinogens;Auerbach;Nature,1976
5. Evidence for at least four Fanconi anaemia genes including FACC on chromosome 9;Strathdee;Nat. Genet.,1992
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