Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
5
pubmed:dateCreated
1980-3-17
pubmed:abstractText
This report describes a Japanese family have two Rhmod members, and two sibs with slightly depressed Rh antigens. It is proposed that the Rhmod and the depressed Rh antigen phenotypes are due to regulator genes in homozygous or heterozygous condition, respectively. The two Rhmod members showed mild reticulocytosis, stomatocytosis, slight anisocytosis, slight hyperchromia and slight punctate basophilia without anaemia. Scanning electron microscopy showed their red cells to be small and of bowl shape. Increased fragility of their erythrocytes was demonstrated by dynamic osmofragility testing using a coil planet centrifuge.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
0042-9007
pubmed:author
pubmed:issnType
Print
pubmed:volume
37
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
296-304
pubmed:dateRevised
2004-11-17
pubmed:meshHeading
pubmed:year
1979
pubmed:articleTitle
A Japanese Rhmod family: serological and haematological observations.
pubmed:publicationType
Journal Article