000 01538 a2200409 4500
005 20250513220237.0
264 0 _c20001019
008 200010s 0 0 eng d
022 _a0049-3848
024 7 _a10.1016/s0049-3848(00)00254-1
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aConroy, J M
245 0 0 _aThe allele frequency of mutations in four genes that confer enhanced susceptibility to venous thromboembolism in an unselected group of New York State newborns.
_h[electronic resource]
260 _bThrombosis research
_cAug 2000
300 _a317-24 p.
_bdigital
500 _aPublication Type: Journal Article
650 0 4 _a5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase
_xgenetics
650 0 4 _aGene Frequency
_xgenetics
650 0 4 _aGenetic Predisposition to Disease
650 0 4 _aHeterozygote
650 0 4 _aHomozygote
650 0 4 _aHumans
650 0 4 _aInfant, Newborn
_xblood
650 0 4 _aMethylenetetrahydrofolate Reductase (NADPH2)
650 0 4 _aMutation
_xgenetics
650 0 4 _aNew York
_xepidemiology
650 0 4 _aOxidoreductases Acting on CH-NH Group Donors
_xgenetics
650 0 4 _aProthrombin
_xgenetics
650 0 4 _aRacial Groups
_xgenetics
650 0 4 _aThromboembolism
_xethnology
650 0 4 _aVenous Thrombosis
_xethnology
700 1 _aTrivedi, G
700 1 _aSovd, T
700 1 _aCaggana, M
773 0 _tThrombosis research
_gvol. 99
_gno. 4
_gp. 317-24
856 4 0 _uhttps://doi.org/10.1016/s0049-3848(00)00254-1
_zAvailable from publisher's website
999 _c10911293
_d10911293