| 000 | 01573 a2200481 4500 | ||
|---|---|---|---|
| 005 | 20250516233319.0 | ||
| 264 | 0 | _c20150604 | |
| 008 | 201506s 0 0 eng d | ||
| 022 | _a1532-432X | ||
| 024 | 7 |
_a10.3109/03630269.2014.948186 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aMarsella, Maria | |
| 245 | 0 | 0 |
_aCharacterization of Hb Calvino (HBB: c.406G > A): a new silent β-globin gene variant found in coexistence with α-thalassemia in a family of African origin. _h[electronic resource] |
| 260 |
_bHemoglobin _c2014 |
||
| 300 |
_a369-72 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article | ||
| 650 | 0 | 4 | _aAmino Acid Substitution |
| 650 | 0 | 4 |
_aAngola _xethnology |
| 650 | 0 | 4 | _aChild, Preschool |
| 650 | 0 | 4 | _aCodon |
| 650 | 0 | 4 | _aFathers |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGene Deletion |
| 650 | 0 | 4 |
_aHemoglobins, Abnormal _xanalysis |
| 650 | 0 | 4 | _aHeterozygote |
| 650 | 0 | 4 | _aHomozygote |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aItaly |
| 650 | 0 | 4 | _aPoint Mutation |
| 650 | 0 | 4 | _aSeverity of Illness Index |
| 650 | 0 | 4 | _aSiblings |
| 650 | 0 | 4 |
_aalpha-Thalassemia _xblood |
| 650 | 0 | 4 |
_abeta-Globins _xanalysis |
| 700 | 1 | _aSalvagno, Gianluca | |
| 700 | 1 | _aDolcini, Bernadetta | |
| 700 | 1 | _aFerlini, Alessandra | |
| 700 | 1 | _aRavani, Anna | |
| 700 | 1 | _aHarteveld, Cornelis L | |
| 700 | 1 | _aGiordano, Piero C | |
| 700 | 1 | _aBorgna-Pignatti, Caterina | |
| 773 | 0 |
_tHemoglobin _gvol. 38 _gno. 5 _gp. 369-72 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.3109/03630269.2014.948186 _zAvailable from publisher's website |
| 999 |
_c24191256 _d24191256 |
||