| 000 | 01526 a2200481 4500 | ||
|---|---|---|---|
| 005 | 20250512113054.0 | ||
| 264 | 0 | _c19740626 | |
| 008 | 197406s 0 0 eng d | ||
| 022 | _a0042-9686 | ||
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aMourant, A E | |
| 245 | 0 | 0 |
_aAssociations between hereditary blood factors and diseases. _h[electronic resource] |
| 260 |
_bBulletin of the World Health Organization _c1973 |
||
| 300 |
_a93-101 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article | ||
| 650 | 0 | 4 |
_aAnemia, Sickle Cell _xgenetics |
| 650 | 0 | 4 | _aBlood Group Antigens |
| 650 | 0 | 4 |
_aChoriocarcinoma _xblood |
| 650 | 0 | 4 |
_aErythroblastosis, Fetal _xblood |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGene Frequency |
| 650 | 0 | 4 |
_aGenetic Diseases, Inborn _xepidemiology |
| 650 | 0 | 4 | _aGenetics, Population |
| 650 | 0 | 4 |
_aGlucosephosphate Dehydrogenase Deficiency _xgenetics |
| 650 | 0 | 4 |
_aGoiter _xcomplications |
| 650 | 0 | 4 | _aHaptoglobins |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aInfant, Newborn |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMolecular Biology |
| 650 | 0 | 4 | _aMutation |
| 650 | 0 | 4 |
_aPeptic Ulcer _xblood |
| 650 | 0 | 4 | _aPolymorphism, Genetic |
| 650 | 0 | 4 | _aPregnancy |
| 650 | 0 | 4 |
_aSmallpox _xblood |
| 650 | 0 | 4 |
_aStomach Neoplasms _xblood |
| 650 | 0 | 4 |
_aTaste Disorders _xcomplications |
| 650 | 0 | 4 |
_aThalassemia _xgenetics |
| 650 | 0 | 4 |
_aThromboembolism _xblood |
| 650 | 0 | 4 | _aTransferrin |
| 650 | 0 | 4 |
_aVaccinia _xblood |
| 773 | 0 |
_tBulletin of the World Health Organization _gvol. 49 _gno. 1 _gp. 93-101 |
|
| 999 |
_c4549332 _d4549332 |
||