Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
1972-10-3
pubmed:language
fre
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
0029-4810
pubmed:author
pubmed:issnType
Print
pubmed:volume
12
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
101-10
pubmed:dateRevised
2004-11-17
pubmed:meshHeading
pubmed-meshheading:4262128-Adolescent, pubmed-meshheading:4262128-Adult, pubmed-meshheading:4262128-Agammaglobulinemia, pubmed-meshheading:4262128-Aged, pubmed-meshheading:4262128-Blood Group Antigens, pubmed-meshheading:4262128-Blood Protein Electrophoresis, pubmed-meshheading:4262128-Child, pubmed-meshheading:4262128-Child, Preschool, pubmed-meshheading:4262128-Female, pubmed-meshheading:4262128-Humans, pubmed-meshheading:4262128-Hypersensitivity, Delayed, pubmed-meshheading:4262128-Immunoelectrophoresis, pubmed-meshheading:4262128-Immunoglobulin A, pubmed-meshheading:4262128-Immunoglobulin G, pubmed-meshheading:4262128-Immunoglobulin M, pubmed-meshheading:4262128-Immunoglobulins, pubmed-meshheading:4262128-Infant, pubmed-meshheading:4262128-Infant, Newborn, pubmed-meshheading:4262128-Male, pubmed-meshheading:4262128-Middle Aged, pubmed-meshheading:4262128-Pedigree
pubmed:articleTitle
[Study of a case of severe congenital primary, non-sex-linked hypogammaglobulinemia of probable genetic origin. Familial survey].
pubmed:publicationType
Journal Article