E A Murphy. Show Affiliations »
Abstract
Mesh: See more » ChildColor Vision Defects/geneticsCounselingErythroblastosis, Fetal/geneticsEugenicsFemaleGlucosephosphate Dehydrogenase Deficiency/geneticsHemophilia A/geneticsHomocystinuria/geneticsHumansHuntington Disease/geneticsLipidoses/geneticsMaleMathematicsMuscular Dystrophies/geneticsMutationPedigreePregnancy
Year: 1968 PMID: 4229313 DOI: 10.1016/s0022-3476(68)80415-9
Source DB: PubMed Journal: J Pediatr ISSN: 0022-3476 Impact factor: 4.406