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Heterogeneous Spectrum Of Mutations In The Fanconi Anaemia Group A Gene
(Stockton Press, 1999)
Fanconi anaemia (FA) is a genetically heterogeneous autosomal recessive disorder associated with chromosomal fragility, bone-marrow failure, congenital abnormalities and cancer. The gene for complementation group A (FAA), ...
The Relative Levels Of Alpha(2)-, Alpha(1)-, And Zeta-Mrna In Hb H Patients With Different Deletional And Nondeletional Alpha-Thalassemia Determinants
(Elsevier Science Bv, 1996)
We have analyzed the alpha(2)/alpha(1)-, alpha/beta-, zeta/(alpha + zeta)-mRNA ratios in the: retic-ulocytes of 40 patients with Hb H disease. 21 patients had deletional Hb H disease (- - / - alpha), namely combinations ...
The Fanconi Anemia Group E Gene, Fance, Maps to Chromosome 6P
(Univ Chicago Press, 1999)
Fanconi anemia (FA) is a genetically heterogeneous autosomal recessive disease with bone marrow failure and predisposition to cancer as major features, often accompanied by developmental anomalies. The cells of patients ...