000 01170 a2200313 4500
005 20250516121724.0
264 0 _c20130605
008 201306s 0 0 eng d
022 _a1096-7206
024 7 _a10.1016/j.ymgme.2012.10.016
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aMcCandless, Shawn E
245 0 0 _aSequencing from dried blood spots in infants with "false positive" newborn screen for MCAD deficiency.
_h[electronic resource]
260 _bMolecular genetics and metabolism
_cJan 2013
300 _a51-5 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, N.I.H., Extramural
650 0 4 _aAcyl-CoA Dehydrogenase
_xblood
650 0 4 _aFalse Positive Reactions
650 0 4 _aHumans
650 0 4 _aInfant, Newborn
650 0 4 _aLipid Metabolism, Inborn Errors
_xblood
650 0 4 _aNeonatal Screening
_xmethods
700 1 _aChandrasekar, Ram
700 1 _aLinard, Sharon
700 1 _aKikano, Sandra
700 1 _aRice, Lorrie
773 0 _tMolecular genetics and metabolism
_gvol. 108
_gno. 1
_gp. 51-5
856 4 0 _uhttps://doi.org/10.1016/j.ymgme.2012.10.016
_zAvailable from publisher's website
999 _c22263451
_d22263451