pubmed-article:1379344 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:1379344 | lifeskim:mentions | umls-concept:C0678804 | lld:lifeskim |
pubmed-article:1379344 | lifeskim:mentions | umls-concept:C0013080 | lld:lifeskim |
pubmed-article:1379344 | lifeskim:mentions | umls-concept:C1858460 | lld:lifeskim |
pubmed-article:1379344 | lifeskim:mentions | umls-concept:C0220908 | lld:lifeskim |
pubmed-article:1379344 | lifeskim:mentions | umls-concept:C0162491 | lld:lifeskim |
pubmed-article:1379344 | lifeskim:mentions | umls-concept:C1524063 | lld:lifeskim |
pubmed-article:1379344 | pubmed:issue | 9 | lld:pubmed |
pubmed-article:1379344 | pubmed:dateCreated | 1992-9-2 | lld:pubmed |
pubmed-article:1379344 | pubmed:abstractText | Approximately 35 percent of all cases of Down's syndrome in fetuses can be detected by measuring maternal serum alpha-fetoprotein during the second trimester in the general population of pregnant women. Recent case-control studies indicate that this detection rate could be approximately doubled by measuring serum levels of unconjugated estriol and chorionic gonadotropin, which are abnormally low and abnormally high, respectively, in women carrying fetuses affected by Down's syndrome. | lld:pubmed |
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pubmed-article:1379344 | pubmed:language | eng | lld:pubmed |
pubmed-article:1379344 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:1379344 | pubmed:citationSubset | AIM | lld:pubmed |
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pubmed-article:1379344 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:1379344 | pubmed:month | Aug | lld:pubmed |
pubmed-article:1379344 | pubmed:issn | 0028-4793 | lld:pubmed |
pubmed-article:1379344 | pubmed:author | pubmed-author:HaddowJ EJE | lld:pubmed |
pubmed-article:1379344 | pubmed:author | pubmed-author:WilliamsJJ | lld:pubmed |
pubmed-article:1379344 | pubmed:author | pubmed-author:CanickJ AJA | lld:pubmed |
pubmed-article:1379344 | pubmed:author | pubmed-author:KnightG JGJ | lld:pubmed |
pubmed-article:1379344 | pubmed:author | pubmed-author:PulkkinenAA | lld:pubmed |
pubmed-article:1379344 | pubmed:author | pubmed-author:PalomakiG EGE | lld:pubmed |
pubmed-article:1379344 | pubmed:author | pubmed-author:SallerD NDNJr | lld:pubmed |
pubmed-article:1379344 | pubmed:author | pubmed-author:BowersG BGB | lld:pubmed |
pubmed-article:1379344 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:1379344 | pubmed:day | 27 | lld:pubmed |
pubmed-article:1379344 | pubmed:volume | 327 | lld:pubmed |
pubmed-article:1379344 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:1379344 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:1379344 | pubmed:pagination | 588-93 | lld:pubmed |
pubmed-article:1379344 | pubmed:dateRevised | 2010-3-24 | lld:pubmed |
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pubmed-article:1379344 | pubmed:year | 1992 | lld:pubmed |
pubmed-article:1379344 | pubmed:articleTitle | Prenatal screening for Down's syndrome with use of maternal serum markers. | lld:pubmed |
pubmed-article:1379344 | pubmed:affiliation | Foundation for Blood Research, Scarborough, Me. 04070-0190. | lld:pubmed |
pubmed-article:1379344 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:1379344 | pubmed:publicationType | Comparative Study | lld:pubmed |
pubmed-article:1379344 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
pubmed-article:1379344 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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