000 | 01232 a2200397 4500 | ||
---|---|---|---|
005 | 20250512090429.0 | ||
264 | 0 | _c19710526 | |
008 | 197105s 0 0 eng d | ||
022 | _a0140-6736 | ||
024 | 7 |
_a10.1016/s0140-6736(71)91992-1 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aMilner, P F | |
245 | 0 | 0 |
_aHaemoglobin-H disease due to a unique haemoglobin variant with an elongated alpha-chain. _h[electronic resource] |
260 |
_bLancet (London, England) _cApr 1971 |
||
300 |
_a729-32 p. _bdigital |
||
500 | _aPublication Type: Journal Article | ||
650 | 0 | 4 | _aAdolescent |
650 | 0 | 4 | _aAdult |
650 | 0 | 4 | _aChild |
650 | 0 | 4 | _aChild, Preschool |
650 | 0 | 4 | _aElectrophoresis |
650 | 0 | 4 | _aFemale |
650 | 0 | 4 |
_aHemoglobinopathies _xgenetics |
650 | 0 | 4 |
_aHemoglobins, Abnormal _xanalysis |
650 | 0 | 4 | _aHeterozygote |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 | _aMale |
650 | 0 | 4 | _aMethods |
650 | 0 | 4 | _aMiddle Aged |
650 | 0 | 4 | _aPedigree |
650 | 0 | 4 |
_aThalassemia _xgenetics |
700 | 1 | _aClegg, J B | |
700 | 1 | _aWeatherall, D J | |
773 | 0 |
_tLancet (London, England) _gvol. 1 _gno. 7702 _gp. 729-32 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1016/s0140-6736(71)91992-1 _zAvailable from publisher's website |
999 |
_c4107098 _d4107098 |