000 01663 a2200445 4500
005 20250513082053.0
264 0 _c19930611
008 199306s 0 0 eng d
022 _a0939-4974
024 7 _a10.1515/cclm.1993.31.3.121
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aVerstraeten, L
245 0 0 _aBiochemical diagnosis of a fatal case of Günther's disease in a newborn with hydrops foetalis.
_h[electronic resource]
260 _bEuropean journal of clinical chemistry and clinical biochemistry : journal of the Forum of European Clinical Chemistry Societies
_cMar 1993
300 _a121-8 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aAminolevulinic Acid
_xurine
650 0 4 _aErythrocytes
_xchemistry
650 0 4 _aFeces
_xchemistry
650 0 4 _aHumans
650 0 4 _aHydrops Fetalis
_xcomplications
650 0 4 _aInfant, Newborn
650 0 4 _aInfant, Premature, Diseases
_xdiagnosis
650 0 4 _aLymphocytes
_xchemistry
650 0 4 _aMale
650 0 4 _aMutation
650 0 4 _aPorphyria, Erythropoietic
_xcomplications
650 0 4 _aPorphyrins
_xanalysis
700 1 _aVan Regemorter, N
700 1 _aPardou, A
700 1 _ade Verneuil, H
700 1 _aDa Silva, V
700 1 _aRodesch, F
700 1 _aVermeylen, D
700 1 _aDonner, C
700 1 _aNoël, J C
700 1 _aNordmann, Y
773 0 _tEuropean journal of clinical chemistry and clinical biochemistry : journal of the Forum of European Clinical Chemistry Societies
_gvol. 31
_gno. 3
_gp. 121-8
856 4 0 _uhttps://doi.org/10.1515/cclm.1993.31.3.121
_zAvailable from publisher's website
999 _c8489327
_d8489327