Fanconi anemia in Tunisia: high prevalence of group A and identification of new FANCA mutations. [electronic resource]
Producer: 20031006Description: 352-61 p. digitalISSN:- 1434-5161
- Alleles
- Base Sequence
- Chromosome Mapping
- DNA Mutational Analysis
- DNA, Complementary -- metabolism
- DNA-Binding Proteins
- Exons
- Family Health
- Fanconi Anemia -- genetics
- Fanconi Anemia Complementation Group A Protein
- Female
- Gene Deletion
- Genetic Linkage
- Genetic Markers
- Genotype
- Haplotypes
- Homozygote
- Humans
- Introns
- Lod Score
- Male
- Microsatellite Repeats
- Molecular Sequence Data
- Mutation
- Phenotype
- Polymorphism, Genetic
- Proteins -- genetics
- Sequence Analysis, DNA
- Time Factors
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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