Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
1970-10-15
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
0007-1048
pubmed:author
pubmed:issnType
Print
pubmed:volume
19
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
179-92
pubmed:dateRevised
2004-11-17
pubmed:meshHeading
pubmed-meshheading:4989292-Adult, pubmed-meshheading:4989292-Aged, pubmed-meshheading:4989292-Blood Coagulation Disorders, pubmed-meshheading:4989292-Blood Coagulation Tests, pubmed-meshheading:4989292-Diagnosis, Differential, pubmed-meshheading:4989292-Factor VII Deficiency, pubmed-meshheading:4989292-Factor X, pubmed-meshheading:4989292-Female, pubmed-meshheading:4989292-Genes, Recessive, pubmed-meshheading:4989292-Heterozygote, pubmed-meshheading:4989292-Humans, pubmed-meshheading:4989292-Hypoprothrombinemias, pubmed-meshheading:4989292-Immunodiffusion, pubmed-meshheading:4989292-Male, pubmed-meshheading:4989292-Middle Aged, pubmed-meshheading:4989292-Neutralization Tests, pubmed-meshheading:4989292-Prothrombin, pubmed-meshheading:4989292-Prothrombin Time, pubmed-meshheading:4989292-Thromboplastin
pubmed:year
1970
pubmed:articleTitle
A "new" congenital haemorrhagic condition due to the presence of an abnormal factor X (factor X Friuli): study of a large kindred.
pubmed:publicationType
Journal Article