Adult onset of a Thalassemia intermedia genotype in association with a -alpha-3.7 homozygosity. Hb G-Accra [beta73(e17)Asp-->Asn] in combination with beta- and alpha-thalassemia in the same family.

van der Padt, Annemiek; Bouva, Marelle; Auwerda, Johannes J A; Dees, Adriaan; Harteveld, Cornelis L; Giordano, Piero C

van der Padt, Annemiek; Bouva, Marelle; Auwerda, Johannes J A; Dees, Adriaan; Harteveld, Cornelis L; Giordano, Piero C.

Affiliation

van der Padt A; Department of Internal Medicine, Ikazia Hospital, Rotterdam, The Netherlands.

Hemoglobin ; 29(4): 269-76, 2005.

Article in En | MEDLINE | ID: mdl-16370487

Subject(s)

Hemoglobins, Abnormal/genetics; alpha-Thalassemia/genetics; beta-Thalassemia/genetics; Adult; Age of Onset; DNA Mutational Analysis; Family Health; Fetal Hemoglobin/analysis; Genotype; Humans; Lymphatic Diseases; Male; Point Mutation; alpha-Thalassemia/diagnosis; beta-Thalassemia/diagnosis

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Collection: 01-internacional Database: MEDLINE Main subject: Hemoglobins, Abnormal / Beta-Thalassemia / Alpha-Thalassemia Type of study: Diagnostic_studies / Risk_factors_studies Limits: Adult / Humans / Male Language: En Journal: Hemoglobin Year: 2005 Document type: Article Affiliation country: Netherlands Country of publication: United kingdom

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