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Journal of Inherited Metabolic Disease|January 1, 1989
RFLPs of the phenylalanine hydroxylase gene in the Italian populationI Dianzani, L Farinasso, P Fortina, et al.Respiration; International Review of Thoracic Diseases|January 1, 1983
Echocardiographic and hemodynamic assessment of right heart impairment in chronic obstructive lung diseaseL Bertoli, G Rizzato, G Sala, et al.European Journal of Pediatrics|January 28, 2003
Diagnosis of juvenile hemochromatosis in an 11-year-old child combining genetic analysis and non-invasive liver iron quantitationM De Gobbi, R Caruso, F Daraio, et al.The EMBO Journal|November 1, 1984
A molecular study of a family with Greek hereditary persistence of fetal hemoglobin and beta-thalassemiaB Giglioni, C Casini, R Mantovani, et al.British Journal of Haematology|August 1, 1991
A newly-characterized alpha-thalassaemia-1 deletion removes the entire alpha-like globin gene cluster in an Italian familyP Fortina, I Dianzani, A Serra, et al.British Journal of Haematology|October 1, 1982
G gamma and a gamma globin chain synthesis in bone marrow and peripheral blood of beta-thalassaemia homozygotesG Saglio, C Camaschella, A Guerrasio, et al.Tumori|August 1, 1982
Chemotherapy of advanced non-Hodgkin lymphomas: a report of 35 casesG Büchi, U Mazza, C Camaschella, et al.Nature Genetics|May 10, 2000
The gene TFR2 is mutated in a new type of haemochromatosis mapping to 7q22C Camaschella, A Roetto, A Calì, et al.Giornale Italiano Di Cardiologia|January 1, 1980
[The pulmonary artery hypertension in patients with sarcoidosis (author's transl)]G Rizzato, L Bertoli, R Merlini, et al.Genomics|September 15, 1996
Construction of a YAC contig covering human chromosome 6p22P Malaspina, A Roetto, F Trettel, et al.Pageof 11