Statements in which the resource exists as a subject.| Predicate | Object |
|---|
|
rdf:type |
|
|
lifeskim:mentions |
|
|
pubmed:issue |
2
|
|
pubmed:dateCreated |
1972-7-25
|
|
pubmed:language |
eng
|
|
pubmed:journal |
|
|
pubmed:citationSubset |
IM
|
|
pubmed:status |
MEDLINE
|
|
pubmed:issn |
0018-7348
|
|
pubmed:author |
|
|
pubmed:issnType |
Print
|
|
pubmed:volume |
14
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
164-6
|
|
pubmed:dateRevised |
2011-11-17
|
|
pubmed:meshHeading |
pubmed-meshheading:5026850-Blepharoptosis,
pubmed-meshheading:5026850-Chromosome Aberrations,
pubmed-meshheading:5026850-Chromosomes, Human, 21-22 and Y,
pubmed-meshheading:5026850-Dermatoglyphics,
pubmed-meshheading:5026850-Diagnosis, Differential,
pubmed-meshheading:5026850-Face,
pubmed-meshheading:5026850-Fibroblasts,
pubmed-meshheading:5026850-Humans,
pubmed-meshheading:5026850-Hypotension,
pubmed-meshheading:5026850-Infant,
pubmed-meshheading:5026850-Intellectual Disability,
pubmed-meshheading:5026850-Karyotyping,
pubmed-meshheading:5026850-Lymphocytes,
pubmed-meshheading:5026850-Male,
pubmed-meshheading:5026850-Microscopy, Fluorescence,
pubmed-meshheading:5026850-Skin,
pubmed-meshheading:5026850-Skin Abnormalities
|
|
pubmed:year |
1972
|
|
pubmed:articleTitle |
G-deletion syndrome II.
|
|
pubmed:publicationType |
Journal Article
|
