Fregin, Andreas <br/><br/>
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] 

 -  Blood  Nov 2002 
 - 3229-32 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0006-4971 
<br/><br/><label>Standard No.: </label>10.1182/blood-2002-03-0698  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Blood Coagulation Factors--analysis<br/>Centromere--genetics<br/>Child<br/>Chromosome Mapping<br/>Chromosomes, Human, Pair 16--genetics<br/>DNA Mutational Analysis<br/>Drug Resistance--genetics<br/>Female<br/>Genes, Recessive<br/>Genetic Markers<br/>Genotype<br/>Germany<br/>Glutathione Transferase--deficiency<br/>Hemorrhagic Disorders--blood<br/>Humans<br/>Infant, Newborn<br/>Lebanon<br/>Lod Score<br/>Male<br/>Mice<br/>Microsatellite Repeats<br/>Mixed Function Oxygenases--deficiency<br/>Multienzyme Complexes--deficiency<br/>Pedigree<br/>Rats<br/>Species Specificity<br/>Vitamin K--physiology<br/>Vitamin K 1--analogs & derivatives<br/>Vitamin K Epoxide Reductases<br/>Warfarin--pharmacology