| 000 | 01362 a2200409 4500 | ||
|---|---|---|---|
| 005 | 20250513183155.0 | ||
| 264 | 0 | _c19990712 | |
| 008 | 199907s 0 0 eng d | ||
| 022 | _a0363-0269 | ||
| 024 | 7 |
_a10.3109/03630269908996162 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aGrignoli, C R | |
| 245 | 0 | 0 |
_aHb Rio Claro [beta34(B16)Val-->Met]: a novel electrophoretically silent variant found in association with Hb Hasharon [alpha47(CE5)Asp-->His] and alpha-thalassemia-2(-alpha3.7). _h[electronic resource] |
| 260 |
_bHemoglobin _cMay 1999 |
||
| 300 |
_a177-82 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 | _aAspartic Acid |
| 650 | 0 | 4 | _aChild, Preschool |
| 650 | 0 | 4 | _aElectrophoresis |
| 650 | 0 | 4 |
_aHemoglobins, Abnormal _xgenetics |
| 650 | 0 | 4 | _aHistidine |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMethionine |
| 650 | 0 | 4 | _aPoint Mutation |
| 650 | 0 | 4 | _aValine |
| 650 | 0 | 4 |
_aalpha-Thalassemia _xgenetics |
| 700 | 1 | _aWenning, M R | |
| 700 | 1 | _aSonati, M F | |
| 700 | 1 | _aKimura, E M | |
| 700 | 1 | _aArruda, V R | |
| 700 | 1 | _aSaad, S T | |
| 700 | 1 | _aCosta, F F | |
| 773 | 0 |
_tHemoglobin _gvol. 23 _gno. 2 _gp. 177-82 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.3109/03630269908996162 _zAvailable from publisher's website |
| 999 |
_c10294795 _d10294795 |
||