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Proceedings of the National Academy of Sciences of the United States of America|February 12, 1998
In vivo telomere dynamics of human hematopoietic stem cellsR Notaro, A Cimmino, D Tabarini, et al.
Annals of Human Genetics|May 1, 1981
New genetic variants of glucose 6-phosphate dehydrogenase (G6PD) in ItalyG Sansone, L Perroni, U Testa, et al.
Experimental Hematology|January 1, 1994
Retroviral-mediated gene transfer of a mutant H-ras gene into normal human bone marrow alters myeloid cell proliferation and differentiationJ Maher, F Colonna, D Baker, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 29, 1997
A variable domain of delayed replication in FRAXA fragile X chromosomes: X inactivation-like spread of late replicationR S Hansen, T K Canfield, A D Fjeld, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|February 24, 2001
Analysis of replication timing at the FRA10B and FRA16B fragile site lociO Handt, E Baker, S Dayan, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 1, 1985
Tissue-specific levels of human glucose-6-phosphate dehydrogenase correlate with methylation of specific sites at the 3' end of the geneG Battistuzzi, M D'Urso, D Toniolo, et al.
Cancer|October 1, 1991
Analysis of beta, gamma, and delta T-cell receptor genes in mycosis fungoides and Sezary syndromeS J Whittaker, N P Smith, R R Jones, et al.
Annals of Human Genetics|October 1, 1989
A new genetic polymorphism in the 16S ribosomal RNA gene of human mitochondrial DNAA B Mehta, T Vulliamy, E C Gordon-Smith, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 1979
Genetic heterogeneity of "normal" human erythrocyte glucose-6-phosphate dehydrogenase: an isoelectrophoretic polymorphismG Modiano, G Battistuzzi, G J Esan, et al.
British Journal of Haematology|February 13, 2001
PNH cells are as sensitive to T-cell-mediated lysis as their normal counterparts: implications for the pathogenesis of paroxysmal nocturnal haemoglobinuriaA Karadimitris, R Notaro, G Koehne, et al.
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