Homozygous HB Sallanches [α104(G11)CYS→TYR] in a Pakistani Child with HB H Disease

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Veröffentlicht in:Hemoglobin 2000-01, Vol.24 (4), p.355-357
Hauptverfasser: Waye, J. S., Walker, L., Chui, D. H. K., Lafferty, J., Kirby, M.
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creator Waye, J. S.
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Chui, D. H. K.
Lafferty, J.
Kirby, M.
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ispartof Hemoglobin, 2000-01, Vol.24 (4), p.355-357
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recordid cdi_informahealthcare_journals_10_3109_03630260008993145
source MEDLINE; Taylor & Francis Medical Library - CRKN; Taylor & Francis Journals Complete
subjects Anemia, Hemolytic - blood
Anemia, Hemolytic - genetics
Globins - genetics
Hemoglobins, Abnormal - genetics
Homozygote
Humans
Infant
Male
Mutation
Pakistan
title Homozygous HB Sallanches [α104(G11)CYS→TYR] in a Pakistani Child with HB H Disease
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