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M Francese

Showing results (11-20 of 14) with videos related to

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Minerva Pediatrica|June 30, 2005
[Inherited disorders of bilirubin metabolism]F Rossi, M Francese, R M Iodice, et al.
British Journal of Haematology|July 1, 1997
Molecular characterization of G6PD deficiency in Southern Italy: heterogeneity, correlation genotype-phenotype and description of a new variant (G6PD Neapolis)F Alfinito, A Cimmino, F Ferraro, et al.
British Journal of Haematology|June 3, 1998
Frequent de novo monoallelic expression of beta-spectrin gene (SPTB) in children with hereditary spherocytosis and isolated spectrin deficiencyE Miraglia del Giudice, C Lombardi, M Francese, et al.
Hematology (Amsterdam, Netherlands)|November 9, 2005
Impact of excess weight and estrogen receptor gene polymorphisms on clinical course of homozygous beta thalassemiaM Ferrara, S M R Matarese, B Borrelli, et al.
Pageof 2

Showing results (11-20 of 14) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 14 results.
Minerva Pediatrica|June 30, 2005
[Inherited disorders of bilirubin metabolism]F Rossi, M Francese, R M Iodice, et al.
British Journal of Haematology|July 1, 1997
Molecular characterization of G6PD deficiency in Southern Italy: heterogeneity, correlation genotype-phenotype and description of a new variant (G6PD Neapolis)F Alfinito, A Cimmino, F Ferraro, et al.
British Journal of Haematology|June 3, 1998
Frequent de novo monoallelic expression of beta-spectrin gene (SPTB) in children with hereditary spherocytosis and isolated spectrin deficiencyE Miraglia del Giudice, C Lombardi, M Francese, et al.
Hematology (Amsterdam, Netherlands)|November 9, 2005
Impact of excess weight and estrogen receptor gene polymorphisms on clinical course of homozygous beta thalassemiaM Ferrara, S M R Matarese, B Borrelli, et al.
Pageof 2