14 research outputs found
Detection of non-deletional type of hereditary persistence of fetal hemoglobin (HPFH) condition associated with 619 bp β°-thalassemia deletion
No full textThe entire β-globin gene cluster is deleted in a form of τδβ-thalassemia.
No full textWe have used restriction endonuclease mapping to study a deletion involving the beta-globin gene cluster in a Mexican-American family with gamma delta beta-thalassemia. Analysis of DNA polymorphisms demonstrated deletion of the beta-globin gene fro
Heterogeneity of the egammadeltabeta-thalassaemias: characterization of three novel English deletions
No full textSevere Hb S-β°-thalassaemia with a T → C substitution in the donor splice site of the first intron of the β-globin gene
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Chromosomal localization and sequence analysis of a human episomal sequence with in vitro differentiating activity
No full textHigh-frequency deletion event ataprt locus of CHO cells: Detection and characterization of endpoints
No full textA very large spontaneous deletion ataprt locus in CHO cells: Sequence similarities with smallaprt deletions
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