| 000 | 01627 a2200481 4500 | ||
|---|---|---|---|
| 005 | 20250516145500.0 | ||
| 264 | 0 | _c20160215 | |
| 008 | 201602s 0 0 eng d | ||
| 022 | _a1751-553X | ||
| 024 | 7 |
_a10.1111/ijlh.12094 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aAmato, A | |
| 245 | 0 | 0 |
_aInterpreting elevated fetal hemoglobin in pathology and health at the basic laboratory level: new and known γ- gene mutations associated with hereditary persistence of fetal hemoglobin. _h[electronic resource] |
| 260 |
_bInternational journal of laboratory hematology _cFeb 2014 |
||
| 300 |
_a13-9 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Review | ||
| 650 | 0 | 4 | _aAdolescent |
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 | _aBase Sequence |
| 650 | 0 | 4 |
_aFetal Hemoglobin _xgenetics |
| 650 | 0 | 4 |
_aHemoglobin A2 _xgenetics |
| 650 | 0 | 4 | _aHeterozygote |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMolecular Sequence Data |
| 650 | 0 | 4 | _aMutation |
| 650 | 0 | 4 | _aPedigree |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 | _aPolymorphism, Genetic |
| 650 | 0 | 4 | _aPromoter Regions, Genetic |
| 650 | 0 | 4 |
_aalpha-Thalassemia _xdiagnosis |
| 650 | 0 | 4 |
_abeta-Thalassemia _xdiagnosis |
| 650 | 0 | 4 |
_adelta-Thalassemia _xdiagnosis |
| 650 | 0 | 4 |
_agamma-Globins _xgenetics |
| 700 | 1 | _aCappabianca, M P | |
| 700 | 1 | _aPerri, M | |
| 700 | 1 | _aZaghis, I | |
| 700 | 1 | _aGrisanti, P | |
| 700 | 1 | _aPonzini, D | |
| 700 | 1 | _aDi Biagio, P | |
| 773 | 0 |
_tInternational journal of laboratory hematology _gvol. 36 _gno. 1 _gp. 13-9 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1111/ijlh.12094 _zAvailable from publisher's website |
| 999 |
_c22703316 _d22703316 |
||