ISSN:
1432-1203
Quelle:
Springer Online Journal Archives 1860-2000
Thema:
Biologie
,
Medizin
Notizen:
Summary Hypohaptoglobinaemia and ahaptoglobinaemia occurred in three generations, mainly to male members of a family. Also small amounts of haptolobin were detected in most of the female relatives. Haemolytic anaemia seemed unlikely and the glucose 6 phosphate dehydrogenase (G.6.P.D.) activity was normal. The probable genotype of these apparently healthy individuals was Hp 2/Hp 2. These preliminary data might suggest a defect in control of gene expression by steroid hormones.
Materialart:
Digitale Medien
URL:
http://dx.doi.org/10.1007/BF00294926