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Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
|
pubmed:dateCreated |
1992-4-24
|
pubmed:abstractText |
A complex case of trisomy 21-related pulmonary hypoplasia with polyhydramnios and hydrops fetalis is described. The value of antenatal surveillance and genetic counselling is emphasized.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:status |
MEDLINE
|
pubmed:month |
Jan
|
pubmed:issn |
0735-1631
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
9
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
9-10
|
pubmed:dateRevised |
2004-11-17
|
pubmed:meshHeading | |
pubmed:year |
1992
|
pubmed:articleTitle |
Hydrops fetalis, polyhydramnios, pulmonary hypoplasia, and Down syndrome.
|
pubmed:affiliation |
Department of Pediatrics and Neonatology, Grace Hospital, Wayne State University, Detroit, MI 48235.
|
pubmed:publicationType |
Journal Article,
Case Reports
|