Localization of the Gene for Congenital Dyserythropoietic Anemia Type I to a <1-cM Interval on Chromosome 15q15.1-15.3

Congenital dyserythropoietic anemias (CDA) are a rare group of red-blood-cell disorders of unknown etiology that are characterized by ineffective erythropoiesis, pathognomonic cytopathology of the nucleated red blood cells in the bone marrow, and secondary hemochromatosis. In CDA type I, bone-marrow...

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Veröffentlicht in:	American journal of human genetics 1998-05, Vol.62 (5), p.1062-1069
Hauptverfasser:	Tamary, Hannah, Shalmon, Lea, Shalev, Hanna, Halil, Albudar, Dobrushin, Dina, Ashkenazi, Noga, Zoldan, Meira, Resnitzky, Peretz, Korostishevsky, Michael, Bonne-Tamir, Batsheva, Zaizov, Rina
Format:	Artikel
Sprache:	eng
Schlagworte:	Anemia Anemia, Dyserythropoietic, Congenital - genetics Bedouins Biological and medical sciences Chromosome 15 Chromosomes, Human, Pair 15 Congential dyserythropoietic anemia type 1 Female Haplotypes Hematologic and hematopoietic diseases Humans Linkage analysis Linkage Disequilibrium Male Medical sciences Mutation age Other diseases. Hematologic involvement in other diseases Pedigree Sequence Analysis, DNA
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