Matches in Nanopublications for { ?s ?p "[We enrolled 49 unrelated Caucasian women with a history of two consecutive or three to six nonconsecutive early pregnancy losses and 48 unrelated parous healthy controls without a history of pregnancy loss and evaluated them for the following genetic variants: the factor V Leiden and prothrombin G20210A gene mutations, the methylenetetrahydrofolate reductase C677T and A1298C polymorphisms, and the PAI-1 4G/5G and FXIII Val34Leu polymorphisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP477695.RAX2aCpgThnBWLHtrENR6p-W1ZAGGvu448l7aIhrPUjvE130_assertion description "[We enrolled 49 unrelated Caucasian women with a history of two consecutive or three to six nonconsecutive early pregnancy losses and 48 unrelated parous healthy controls without a history of pregnancy loss and evaluated them for the following genetic variants: the factor V Leiden and prothrombin G20210A gene mutations, the methylenetetrahydrofolate reductase C677T and A1298C polymorphisms, and the PAI-1 4G/5G and FXIII Val34Leu polymorphisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP477695.RAX2aCpgThnBWLHtrENR6p-W1ZAGGvu448l7aIhrPUjvE130_provenance.
- NP398826.RAVoY2dmh-A364TI06WRPgWxLdAJKMAeL3aqCT_uzK5zI130_assertion description "[We enrolled 49 unrelated Caucasian women with a history of two consecutive or three to six nonconsecutive early pregnancy losses and 48 unrelated parous healthy controls without a history of pregnancy loss and evaluated them for the following genetic variants: the factor V Leiden and prothrombin G20210A gene mutations, the methylenetetrahydrofolate reductase C677T and A1298C polymorphisms, and the PAI-1 4G/5G and FXIII Val34Leu polymorphisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP398826.RAVoY2dmh-A364TI06WRPgWxLdAJKMAeL3aqCT_uzK5zI130_provenance.
- NP389817.RAh6owbBZjebHY9qRt9av1nEBptrwae-YCZrxwmrTsbiw130_assertion description "[We enrolled 49 unrelated Caucasian women with a history of two consecutive or three to six nonconsecutive early pregnancy losses and 48 unrelated parous healthy controls without a history of pregnancy loss and evaluated them for the following genetic variants: the factor V Leiden and prothrombin G20210A gene mutations, the methylenetetrahydrofolate reductase C677T and A1298C polymorphisms, and the PAI-1 4G/5G and FXIII Val34Leu polymorphisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP389817.RAh6owbBZjebHY9qRt9av1nEBptrwae-YCZrxwmrTsbiw130_provenance.
- NP391786.RAOKTSpZcXZvDU1GdUAV5FxAqbI2k7mxS2RKGhALXDd2M130_assertion description "[We enrolled 49 unrelated Caucasian women with a history of two consecutive or three to six nonconsecutive early pregnancy losses and 48 unrelated parous healthy controls without a history of pregnancy loss and evaluated them for the following genetic variants: the factor V Leiden and prothrombin G20210A gene mutations, the methylenetetrahydrofolate reductase C677T and A1298C polymorphisms, and the PAI-1 4G/5G and FXIII Val34Leu polymorphisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP391786.RAOKTSpZcXZvDU1GdUAV5FxAqbI2k7mxS2RKGhALXDd2M130_provenance.
- NP398824.RAwj4Tn1OrnIN2jwnYyK3MDurleHUQQSs39MJX9OUTtv8130_assertion description "[We enrolled 49 unrelated Caucasian women with a history of two consecutive or three to six nonconsecutive early pregnancy losses and 48 unrelated parous healthy controls without a history of pregnancy loss and evaluated them for the following genetic variants: the factor V Leiden and prothrombin G20210A gene mutations, the methylenetetrahydrofolate reductase C677T and A1298C polymorphisms, and the PAI-1 4G/5G and FXIII Val34Leu polymorphisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP398824.RAwj4Tn1OrnIN2jwnYyK3MDurleHUQQSs39MJX9OUTtv8130_provenance.