I Oberlé, J L Mandel. Show Affiliations »
Abstract
Entities: Disease Species
Mesh: See more » Chromosome MappingFactor IX/geneticsFactor VII/geneticsFragile X Syndrome/diagnosisFragile X Syndrome/geneticsGenetic LinkageHemophilia A/diagnosisHemophilia A/geneticsHemophilia B/diagnosisHemophilia B/geneticsHumansMutationPolymorphism, Restriction Fragment LengthPrenatal DiagnosisRecombination, GeneticSex Chromosome Aberrations/geneticsX Chromosome/ultrastructure
Substances: See more » Factor VIIFactor IX
Year: 1986 PMID: 2875934
Source DB: PubMed Journal: Horiz Biochem Biophys ISSN: 0096-2708