000 01455 a2200469 4500
005 20250514032947.0
264 0 _c20030204
008 200302s 0 0 eng d
022 _a0340-6199
024 7 _a10.1007/s004310100818
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aKoch, Andreas
245 0 0 _aHypoparathyroidism in conotruncal heart defects.
_h[electronic resource]
260 _bEuropean journal of pediatrics
_cApr 2002
300 _a208-11 p.
_bdigital
500 _aPublication Type: Journal Article
650 0 4 _aAdolescent
650 0 4 _aAdult
650 0 4 _aCalcium
_xblood
650 0 4 _aChild
650 0 4 _aChild, Preschool
650 0 4 _aChromosome Deletion
650 0 4 _aChromosomes, Human, Pair 22
650 0 4 _aFemale
650 0 4 _aHeart Defects, Congenital
_xblood
650 0 4 _aHumans
650 0 4 _aHypoparathyroidism
_xblood
650 0 4 _aInfant
650 0 4 _aInfant, Newborn
650 0 4 _aMale
650 0 4 _aRetrospective Studies
650 0 4 _aTetralogy of Fallot
_xgenetics
650 0 4 _aTruncus Arteriosus, Persistent
_xgenetics
700 1 _aHofbeck, Michael
700 1 _aBuheitel, Gernot
700 1 _aDörr, Helmuth-Günther
700 1 _aRauch, Anita
700 1 _aRauch, Ralf
700 1 _aSinger, Helmut
773 0 _tEuropean journal of pediatrics
_gvol. 161
_gno. 4
_gp. 208-11
856 4 0 _uhttps://doi.org/10.1007/s004310100818
_zAvailable from publisher's website
999 _c11912638
_d11912638