Congenital haemolytic disease (haemolytic disease of the newborn): a study of 157 cases, with special reference to the morbid anatomy and morbid histology of the disease process and to the pathogenesis of kernicterus
dc.contributor.author
Claireaux, Arthur Edward
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dc.date.accessioned
2018-01-31T11:41:31Z
dc.date.available
2018-01-31T11:41:31Z
dc.date.issued
1949
dc.description.abstract
en
dc.description.abstract
Congenital haemolytic disease is a disease complex which may easily be separated into three more or less distinct clinical entities. These are:
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dc.description.abstract
1. Hydrops foetalis.
2. Icterus gravis neonatorum.
3. Congenital haemolytic anaemia.
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dc.identifier.uri
http://hdl.handle.net/1842/27797
dc.publisher
The University of Edinburgh
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dc.relation.ispartof
Annexe Thesis Digitisation Project 2017 Block 16
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dc.relation.isreferencedby
Already catalogued
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dc.title
Congenital haemolytic disease (haemolytic disease of the newborn): a study of 157 cases, with special reference to the morbid anatomy and morbid histology of the disease process and to the pathogenesis of kernicterus
en
dc.type
Thesis or Dissertation
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dc.type.qualificationlevel
en
dc.type.qualificationname
PhD Doctor of Philosophy
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