Haemoglobin H disease and  -thalassaemia: Clinical haematological and electrophoretic studies in a family from South Lebanon

A family is described in which four sibs are affected with haemoglobin H disease. To our knowledge, this is the first instance where this disorder has been encountered in the Lebanon. In fact only a few cases have so far been reported from the Arab world. All four sibs had typical haemoglobin H band...

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Veröffentlicht in:	Journal of medical genetics 1974-09, Vol.11 (3), p.275-279
Hauptverfasser:	Shahid, M. J., Khouri, F. P., Sahli, I. F.
Format:	Artikel
Sprache:	eng
Online-Zugang:	Volltext
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