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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
3
|
| pubmed:dateCreated |
1981-7-20
|
| pubmed:abstractText |
A terminal deletion of the long arm of chromosome 7 is identified in a boy observed from birth to age 6 months. Eleven previously reported cases were reviewed. Eleven previously reported cases were reviewed. The most common features are microcephaly with brachycephaly, prominent forehead, large ears, a nose with bulbous tip, overlapping toes, genital abnormalities in the males and excess of subcutaneous tissue. Delayed mental and physical development is a general rule but visceral malformations seem uncommon.
|
| pubmed:language |
fre
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:status |
MEDLINE
|
| pubmed:month |
Mar
|
| pubmed:issn |
0003-9764
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
38
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
177-80
|
| pubmed:dateRevised |
2006-11-15
|
| pubmed:meshHeading |
pubmed-meshheading:7235841-Abnormalities, Multiple,
pubmed-meshheading:7235841-Chromosome Aberrations,
pubmed-meshheading:7235841-Chromosome Deletion,
pubmed-meshheading:7235841-Chromosomes, Human, 6-12 and X,
pubmed-meshheading:7235841-Humans,
pubmed-meshheading:7235841-Infant, Newborn,
pubmed-meshheading:7235841-Male
|
| pubmed:year |
1981
|
| pubmed:articleTitle |
[Monosomy 7qter (author's transl)].
|
| pubmed:publicationType |
Journal Article,
English Abstract,
Case Reports
|