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Haematologica|July 11, 1998
Molecular genetics and control of iron metabolism in hemochromatosisA Pietrangelo, C CamaschellaBritish Journal of Haematology|May 1, 1987
A benign form of thalassaemia intermedia may be determined by the interaction of triplicated alpha locus and heterozygous beta-thalassaemiaC Camaschella, M T Bertero, A Serra, et al.Human Genetics|April 1, 1995
New polymorphisms and markers in the HLA class I region: relevance to hereditary hemochromatosis (HFE)A Totaro, A Grifa, A Roetto, et al.Blood|April 21, 2001
New mutations inactivating transferrin receptor 2 in hemochromatosis type 3A Roetto, A Totaro, A Piperno, et al.Haematologica|January 1, 1997
Hereditary hemochromatosis: recent advances in molecular genetics and clinical managementC Camaschella, A PipernoHepatology (Baltimore, Md.)|July 1, 1996
The ancestral hemochromatosis haplotype is associated with a severe phenotype expression in Italian patientsA Piperno, C Arosio, S Fargion, et al.American Journal of Human Genetics|April 1, 1997
Mutation analysis of the HLA-H gene in Italian hemochromatosis patientsM Carella, L D'Ambrosio, A Totaro, et al.Genomics|February 1, 1996
Hereditary hemochromatosis: generation of a transcription map within a refined and extended map of the HLA class I regionA Totaro, J M Rommens, A Grifa, et al.European Journal of Human Genetics : EJHG|February 5, 1998
Juvenile and adult hemochromatosis are distinct genetic disordersC Camaschella, A Roetto, M Cicilano, et al.Pageof 25