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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
1
|
| pubmed:dateCreated |
1990-3-9
|
| pubmed:abstractText |
We describe a premature male infant with an interstitial deletion of 7q [46,XY,del(7) (pter----q21.3::q31.3----qter]. Manifestations include absence of lower limbs, unilateral ectrodactyly, facial anomalies, gingival hyperplasia, feeding problems, and atrial septal defect. Chromosome 7 deletions of the q21.3----q31.3 region are reviewed with emphasis on limb anomalies.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:status |
MEDLINE
|
| pubmed:month |
Jan
|
| pubmed:issn |
0148-7299
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
35
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
95-9
|
| pubmed:dateRevised |
2004-11-17
|
| pubmed:meshHeading |
pubmed-meshheading:2301476-Chromosome Banding,
pubmed-meshheading:2301476-Chromosome Deletion,
pubmed-meshheading:2301476-Chromosomes, Human, Pair 7,
pubmed-meshheading:2301476-Ectromelia,
pubmed-meshheading:2301476-Hand Deformities, Congenital,
pubmed-meshheading:2301476-Humans,
pubmed-meshheading:2301476-Infant, Newborn,
pubmed-meshheading:2301476-Male
|
| pubmed:year |
1990
|
| pubmed:articleTitle |
Ectro-amelia syndrome associated with an interstitial deletion of 7q.
|
| pubmed:affiliation |
Division of Genetics, Children's Mercy Hospital, Kansas City, Missouri 64108.
|
| pubmed:publicationType |
Journal Article,
Case Reports
|