A W Morrison. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » AdolescentAdultAgedAntibodiesBirth OrderBlood Group AntigensChildChild, PreschoolChromosome AberrationsChromosome DisordersColor Vision Defects/geneticsDeafness/geneticsEuropean Continental Ancestry GroupFemaleHaptoglobinsHumansMaleMiddle AgedOtosclerosis/epidemiologyOtosclerosis/geneticsOtosclerosis/pathologyPregnancyPregnancy ComplicationsRetinitis Pigmentosa/geneticsSclera/abnormalitiesTaste
Substances: See more » AntibodiesBlood Group AntigensHaptoglobins
Year: 1967 PMID: 5298472 PMCID: PMC2311999
Source DB: PubMed Journal: Ann R Coll Surg Engl ISSN: 0035-8843 Impact factor: 1.891