A T Rundle. Show Affiliations »
Abstract
Entities: Disease Gene
Mesh: See more » Alanine TransaminaseAllelesAminohydrolasesAmylasesChromosome AberrationsChromosome DisordersChromosome MappingCrossing Over, GeneticDown Syndrome/geneticsElectrophoresis, Starch GelGenotypeHaptoglobins/bloodHumansImmunoelectrophoresisIntellectual Disability/geneticsMeiosisModels, BiologicalPepsinogens/urinePhenotypePhosphoglucomutasePolymorphism, GeneticTrisomy
Substances: See more » HaptoglobinsPepsinogensAlanine TransaminaseAmylasesAminohydrolasesPhosphoglucomutase
Year: 1973 PMID: 4277737 DOI: 10.1111/j.1399-0004.1973.tb01942.x
Source DB: PubMed Journal: Clin Genet ISSN: 0009-9163 Impact factor: 4.438