Compound Heterozygosity for a Mild β+ and a Rare β°-Thalassemia Allele

Autor:	J. H. Wisse, J. F. Codrington, Ferdane Kutlar, J. Anijs, Titus H.J. Huisman, H.-W. Li, F. A. Codrington, M. Ramachandran
Rok vydání:	1990
Předmět:	Genetics Mutation Thalassemia Hematology General Medicine Biology Compound heterozygosity medicine.disease medicine.disease_cause Molecular biology Loss of heterozygosity Hemoglobinopathy medicine Hemoglobin Globin Allele
Zdroj:	Acta Haematologica. 84:135-138
ISSN:	1421-9662 0001-5792
DOI:	10.1159/000205050
Popis:	Hematological and hemoglobin composition data are presented for 14 members of a Surinam family (and for 1 unrelated subject) with either a β-thalassemia heterozygosity [5 with the -29 (A – G) β+
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::f6a77d849e60145b146ec423ed275374 https://doi.org/10.1159/000205050 Zobrazit plný text záznamu