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dc.contributor.authorMunro, Thomas A.en
dc.date.accessioned2019-02-15T14:38:22Z
dc.date.available2019-02-15T14:38:22Z
dc.date.issued1940en
dc.identifier.urihttp://hdl.handle.net/1842/35434
dc.description.abstractThis thesis analyses 43 families with 86 cases of phenylketonuria, a rare metabolic disorder always associated with mental defect and occurring in about 4 per 100,000 persons, defines the symptomatology, discusses the pathology and biochemistry, proves the inheritance of the disease as a Mendelian recessive Character, records the presence of other mental disorders in the families and reviews the literature.en
dc.publisherThe University of Edinburghen
dc.relation.ispartofAnnexe Thesis Digitisation Project 2019 Block 22en
dc.relation.isreferencedbyen
dc.titlePhenyleketonuria: a clinical and genetic study of British familiesen
dc.typeThesis or Dissertationen
dc.type.qualificationlevelDoctoralen
dc.type.qualificationnameMD Doctor of Medicineen


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