G M Martin, H Hoehn. Show Affiliations »
Abstract
Entities: Species
Mesh: See more » Arteriosclerosis/geneticsChromosome Aberrations/geneticsChromosome DisordersChromosome MappingChromosomes, Human, 1-3CytogeneticsEnvironmentFemaleGenetic Diseases, InbornGenetics, MedicalGenotypeHumansHybrid CellsKaryotypingMaleMetabolism, Inborn Errors/geneticsMolecular BiologyNeoplasms/enzymologyNeoplasms/geneticsNucleic Acid RenaturationPolymorphism, GeneticPrenatal DiagnosisSelection, Genetic
Year: 1974 PMID: 4600308 DOI: 10.1016/s0046-8177(74)80019-5
Source DB: PubMed Journal: Hum Pathol ISSN: 0046-8177 Impact factor: 3.466