| 000 | 01462 a2200421 4500 | ||
|---|---|---|---|
| 005 | 20250515075001.0 | ||
| 264 | 0 | _c20071005 | |
| 008 | 200710s 0 0 eng d | ||
| 022 | _a0363-0269 | ||
| 024 | 7 |
_a10.1080/03630260701459374 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aHarteveld, Cornelis L | |
| 245 | 0 | 0 |
_aHb Zoetermeer: a new mutation on the alpha2 gene inducing an Ala-->Ser substitution at codon 21 is possibly associated with a mild thalassemic phenotype. _h[electronic resource] |
| 260 |
_bHemoglobin _c2007 |
||
| 300 |
_a325-32 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aAmino Acid Substitution |
| 650 | 0 | 4 |
_aGlobins _xgenetics |
| 650 | 0 | 4 |
_aHemoglobins, Abnormal _xchemistry |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMiddle Aged |
| 650 | 0 | 4 | _aMutation |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 | _aPolymerase Chain Reaction |
| 650 | 0 | 4 | _aProtein Conformation |
| 650 | 0 | 4 |
_aThalassemia _xgenetics |
| 700 | 1 | _avan Helden, Willem C H | |
| 700 | 1 | _aBoxma, George L | |
| 700 | 1 | _avan Delft, Peter | |
| 700 | 1 | _aBakker-Verweij, Margaretha | |
| 700 | 1 | _aWajcman, Henri | |
| 700 | 1 | _aZanella-Cleon, Isabelle | |
| 700 | 1 | _aBecchi, Michel | |
| 700 | 1 | _aGiordano, Piero C | |
| 773 | 0 |
_tHemoglobin _gvol. 31 _gno. 3 _gp. 325-32 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1080/03630260701459374 _zAvailable from publisher's website |
| 999 |
_c17187848 _d17187848 |
||