000 01596 a2200493 4500
005 20250515205236.0
264 0 _c20100901
008 201009s 0 0 eng d
022 _a0717-6287
024 7 _a/S0716-97602009000400007
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aCalderón, Juan Francisco
245 0 0 _aVEGFA polymorphisms and cardiovascular anomalies in 22q11 microdeletion syndrome: a case-control and family-based study.
_h[electronic resource]
260 _bBiological research
_c2009
300 _a461-8 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAdolescent
650 0 4 _aAdult
650 0 4 _aChild
650 0 4 _aChild, Preschool
650 0 4 _aDiGeorge Syndrome
_xcomplications
650 0 4 _aFamily
650 0 4 _aFemale
650 0 4 _aGene Frequency
650 0 4 _aHaplotypes
650 0 4 _aHeart Defects, Congenital
_xetiology
650 0 4 _aHumans
650 0 4 _aInfant
650 0 4 _aInfant, Newborn
650 0 4 _aMale
650 0 4 _aPolymorphism, Genetic
_xgenetics
650 0 4 _aVascular Endothelial Growth Factor A
_xgenetics
650 0 4 _aYoung Adult
700 1 _aPuga, Alonso R
700 1 _aGuzmán, M Luisa
700 1 _aAstete, Carmen Paz
700 1 _aArriaza, Marta
700 1 _aAracena, Mariana
700 1 _aAravena, Teresa
700 1 _aSanz, Patricia
700 1 _aRepetto, Gabriela M
773 0 _tBiological research
_gvol. 42
_gno. 4
_gp. 461-8
856 4 0 _uhttps://doi.org//S0716-97602009000400007
_zAvailable from publisher's website
999 _c19511423
_d19511423