A single point mutation is the cause of the Greek form of hereditary persistence of fetal haemoglobin (Q34249835)
scientific article published on August 6, 1992
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(P31) (Q13442814)
(P304) 499-502
(P407) (Q1860)
(P433) 6386
(P478) 358
(P577) Saturday, August 1, 1992
Thursday, August 6, 1992
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(P1476) "A single point mutation is the cause of the Greek form of hereditary persistence of fetal haemoglobin" (language: en)
(P2093) Berry M
Grosveld F
Dillon N
(P2860) (Q34467772)
(Q34467766)
(Q59064800)
(Q29620032)
(Q52241950)
(Q52242246)
(Q52236177)
(Q41584064)
(Q36814647)
(Q36074818)
(Q35244986)
(Q38347504)
(Q36775117)
(Q38338431)
(Q36684177)
(Q52250555)
(Q27860728)
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description scientific article published on August 6, 1992

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