| 000 | 01616 a2200517 4500 | ||
|---|---|---|---|
| 005 | 20250513072518.0 | ||
| 264 | 0 | _c19930805 | |
| 008 | 199308s 0 0 eng d | ||
| 022 | _a0022-2593 | ||
| 024 | 7 |
_a10.1136/jmg.30.5.396 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aWhite, J M | |
| 245 | 0 | 0 |
_aFrequency and clinical significance of erythrocyte genetic abnormalities in Omanis. _h[electronic resource] |
| 260 |
_bJournal of medical genetics _cMay 1993 |
||
| 300 |
_a396-400 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article | ||
| 650 | 0 | 4 | _aAdolescent |
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 | _aAged |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 | _aErythrocyte Indices |
| 650 | 0 | 4 |
_aErythrocytes _xchemistry |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 |
_aFerritins _xanalysis |
| 650 | 0 | 4 |
_aFetal Blood _xcytology |
| 650 | 0 | 4 | _aGene Frequency |
| 650 | 0 | 4 |
_aGlucosephosphate Dehydrogenase _xblood |
| 650 | 0 | 4 |
_aGlucosephosphate Dehydrogenase Deficiency _xepidemiology |
| 650 | 0 | 4 |
_aHemoglobins _xanalysis |
| 650 | 0 | 4 | _aHeterozygote |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aInfant, Newborn |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMiddle Aged |
| 650 | 0 | 4 |
_aOman _xepidemiology |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 |
_aSickle Cell Trait _xepidemiology |
| 650 | 0 | 4 |
_aalpha-Thalassemia _xepidemiology |
| 650 | 0 | 4 |
_abeta-Thalassemia _xepidemiology |
| 700 | 1 | _aChristie, B S | |
| 700 | 1 | _aNam, D | |
| 700 | 1 | _aDaar, S | |
| 700 | 1 | _aHiggs, D R | |
| 773 | 0 |
_tJournal of medical genetics _gvol. 30 _gno. 5 _gp. 396-400 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1136/jmg.30.5.396 _zAvailable from publisher's website |
| 999 |
_c8319982 _d8319982 |
||