000 01457 a2200433 4500
005 20250514001212.0
264 0 _c20011025
008 200110s 0 0 eng d
022 _a0969-1413
024 7 _a10.1136/jms.8.1.8
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aDucrocq, R
245 0 0 _aStrategy linking several analytical methods of neonatal screening for sickle cell disease.
_h[electronic resource]
260 _bJournal of medical screening
_c2001
300 _a8-14 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAnemia, Sickle Cell
_xblood
650 0 4 _aBase Sequence
650 0 4 _aChromatography, High Pressure Liquid
650 0 4 _aChromatography, Ion Exchange
650 0 4 _aDiagnostic Errors
650 0 4 _aGenetic Carrier Screening
650 0 4 _aGenetic Testing
_xmethods
650 0 4 _aGenetic Variation
650 0 4 _aHemoglobin, Sickle
_xgenetics
650 0 4 _aHumans
650 0 4 _aInfant, Newborn
650 0 4 _aNeonatal Screening
_xmethods
650 0 4 _aOligonucleotide Probes
_xgenetics
650 0 4 _aParis
650 0 4 _aSensitivity and Specificity
700 1 _aPascaud, O
700 1 _aBévier, A
700 1 _aFinet, C
700 1 _aBenkerrou, M
700 1 _aElion, J
773 0 _tJournal of medical screening
_gvol. 8
_gno. 1
_gp. 8-14
856 4 0 _uhttps://doi.org/10.1136/jms.8.1.8
_zAvailable from publisher's website
999 _c11305624
_d11305624