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