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Genotype of subjects with borderline hemoglobin A2 levels: implication for beta-thalassemia carrier screening.
Am J Hematol. 1994 Jun;46(2):79-81. doi: 10.1002/ajh.2830460204.
Am J Hematol. 1994.
PMID: 8172199
Normal individuals with high Hb A2 levels.
Gasperini D, Cao A, Paderi L, Barella S, Paglietti E, Perseu L, Loi D, Galanello R.
Gasperini D, et al. Among authors: paderi l.
Br J Haematol. 1993 May;84(1):166-8. doi: 10.1111/j.1365-2141.1993.tb03042.x.
Br J Haematol. 1993.
PMID: 8338770
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Homozygous non-deletion alpha 2 globin gene mutation (initiation codon mutation): clinical and haematological phenotype.
Galanello R, Monne MI, Paderi L, Paglietti E, Atzori G, Addis M, Limongelli O, Macciotta A, Cao A.
Galanello R, et al. Among authors: paderi l.
Br J Haematol. 1991 Sep;79(1):117-9. doi: 10.1111/j.1365-2141.1991.tb08018.x.
Br J Haematol. 1991.
PMID: 1911369
No abstract available.
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Evaluation of an automatic HPLC analyser for thalassemia and haemoglobin variants screening.
Galanello R, Barella S, Gasperini D, Perseu L, Paglietti E, Sollaino C, Paderi L, Pirroni MG, Maccioni L, Mosca A.
Galanello R, et al. Among authors: paderi l.
J Automat Chem. 1995;17(2):73-6. doi: 10.1155/S1463924695000125.
J Automat Chem. 1995.
PMID: 18925016
Free PMC article.
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