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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
2
|
| pubmed:dateCreated |
1986-11-14
|
| pubmed:abstractText |
A male newborn with partial deletion of the short arm of chromosome 3 is described. The patient shares most of the features with the previously reported cases. In addition, cardiac, skeletal and gastrointestinal anomalies not previously reported are described. These characteristics may help in further delineation of the syndrome.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:status |
MEDLINE
|
| pubmed:month |
Aug
|
| pubmed:issn |
0009-9163
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
30
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
127-30
|
| pubmed:dateRevised |
2004-11-17
|
| pubmed:meshHeading |
pubmed-meshheading:3757303-Abnormalities, Multiple,
pubmed-meshheading:3757303-Chromosome Deletion,
pubmed-meshheading:3757303-Chromosomes, Human, Pair 3,
pubmed-meshheading:3757303-Humans,
pubmed-meshheading:3757303-Infant, Newborn,
pubmed-meshheading:3757303-Male,
pubmed-meshheading:3757303-Syndrome
|
| pubmed:year |
1986
|
| pubmed:articleTitle |
Partial deletion of the short arm of chromosome 3: further delineation of the 3p25-3pter syndrome.
|
| pubmed:publicationType |
Journal Article,
Case Reports
|