| 000 | 01483 a2200433 4500 | ||
|---|---|---|---|
| 005 | 20250511122802.0 | ||
| 264 | 0 | _c19800825 | |
| 008 | 198008s 0 0 fre d | ||
| 022 | _a0003-3898 | ||
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aBrivet, M | |
| 245 | 0 | 0 |
_a[Hereditary abnormalities of galactose metabolism: diagnosis and biochemical supervision (author's transl)]. _h[electronic resource] |
| 260 |
_bAnnales de biologie clinique _c1979 |
||
| 300 |
_a259-70 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Review | ||
| 650 | 0 | 4 |
_aBiological Assay _xmethods |
| 650 | 0 | 4 |
_aCarbohydrate Epimerases _xdeficiency |
| 650 | 0 | 4 |
_aCarbohydrate Metabolism, Inborn Errors _xdiagnosis |
| 650 | 0 | 4 | _aChromatography, Paper |
| 650 | 0 | 4 |
_aErythrocytes _xenzymology |
| 650 | 0 | 4 |
_aEscherichia coli _xenzymology |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 |
_aGalactokinase _xdeficiency |
| 650 | 0 | 4 |
_aGalactose _xmetabolism |
| 650 | 0 | 4 | _aGalactosemias |
| 650 | 0 | 4 | _aHeterozygote |
| 650 | 0 | 4 | _aHomozygote |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aInfant, Newborn |
| 650 | 0 | 4 |
_aInfant, Newborn, Diseases _xdiagnosis |
| 650 | 0 | 4 |
_aNucleotidyltransferases _xdeficiency |
| 650 | 0 | 4 | _aPregnancy |
| 650 | 0 | 4 | _aPrenatal Diagnosis |
| 650 | 0 | 4 |
_aUDPglucose 4-Epimerase _xdeficiency |
| 650 | 0 | 4 |
_aUDPglucose-Hexose-1-Phosphate Uridylyltransferase _xblood |
| 700 | 1 | _aMoatti, N | |
| 700 | 1 | _aLemonnier, A | |
| 773 | 0 |
_tAnnales de biologie clinique _gvol. 37 _gno. 5 _gp. 259-70 |
|
| 999 |
_c258122 _d258122 |
||