|
rdf:type |
|
|
lifeskim:mentions |
|
|
pubmed:issue |
5
|
|
pubmed:dateCreated |
1978-9-25
|
|
pubmed:abstractText |
The limitation of amniocentesis is emphasised by a mother with trisomy 21 who had a baby with a normal karyotype but with malformations. The question is posed whether half the infants of women with trisomy 21 are normal and half have a trisomy. With more observations it may become apparent that there are an excess of children without the trisomy.
|
|
pubmed:language |
fre
|
|
pubmed:journal |
|
|
pubmed:citationSubset |
IM
|
|
pubmed:status |
MEDLINE
|
|
pubmed:month |
May
|
|
pubmed:issn |
0003-9764
|
|
pubmed:author |
|
|
pubmed:issnType |
Print
|
|
pubmed:volume |
35
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
546-50
|
|
pubmed:dateRevised |
2007-11-15
|
|
pubmed:meshHeading |
pubmed-meshheading:150262-Adult,
pubmed-meshheading:150262-Amniocentesis,
pubmed-meshheading:150262-Congenital Abnormalities,
pubmed-meshheading:150262-Down Syndrome,
pubmed-meshheading:150262-Female,
pubmed-meshheading:150262-Humans,
pubmed-meshheading:150262-Infant, Newborn,
pubmed-meshheading:150262-Karyotyping,
pubmed-meshheading:150262-Pregnancy,
pubmed-meshheading:150262-Pregnancy Complications,
pubmed-meshheading:150262-Trisomy
|
|
pubmed:year |
1978
|
|
pubmed:articleTitle |
[Amniocentesis in a woman with trisomy 21 and a fetus with normal karyotype but with abnormalities].
|
|
pubmed:publicationType |
Journal Article,
English Abstract,
Case Reports
|
