Homozygosity mapping of a second gene locus for hereditary combined deficiency of vitamin K-dependent clotting factors to the centromeric region of chromosome 16. [electronic resource]
Producer: 20021210Description: 3229-32 p. digitalISSN:- 0006-4971
- Animals
- Blood Coagulation Factors -- analysis
- Centromere -- genetics
- Child
- Chromosome Mapping
- Chromosomes, Human, Pair 16 -- genetics
- DNA Mutational Analysis
- Drug Resistance -- genetics
- Female
- Genes, Recessive
- Genetic Markers
- Genotype
- Germany
- Glutathione Transferase -- deficiency
- Hemorrhagic Disorders -- blood
- Humans
- Infant, Newborn
- Lebanon
- Lod Score
- Male
- Mice
- Microsatellite Repeats
- Mixed Function Oxygenases -- deficiency
- Multienzyme Complexes -- deficiency
- Pedigree
- Rats
- Species Specificity
- Vitamin K -- physiology
- Vitamin K 1 -- analogs & derivatives
- Vitamin K Epoxide Reductases
- Warfarin -- pharmacology
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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