Author:
Meloni T.,Gallisai D.,Dore A.,Forteleoni G.,Mela G.
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology and Child Health
Reference9 articles.
1. Mazza U, Meloni T, David O, Pich PG, Camaschella C, Saglio G, Ciocca Vasino MA, Guerrasio A, Ricco G (1980) γ-Chain composition in five Italian newborns heterozygous for Hb F Malta G γ 117 His»Arg. Br J Haematol 44:93–99
2. Meloni T, Pilo G, Camardella L, Cancedda F, Lania A, Pepe G, Luzzatto L (1980) Coexistence of three hemoglobins with different a-chains in two unrelated children (with family studies indicating polymorphism in the number of a-globin genes in the Sardinian population). Blood 55:1025–1032
3. Galanello R, Cao A (1979) L'a-talassemia: eterogeneitá, patologia moleculare, genetica, incidenza, aspetti clinici ed ematologici, fisiopatologia, associazione a-tal/varianti emoglobiniche, prevenzione e terapia. Riv Ital Ped 5:457–471
4. Bianco I, Graziani B, Salvini P, Mastromonaco I, Silvestroni E (1972) Frequence et characteres de l'alpha-microcytemie dans les populations de la Sardegne Septentrionale. Nouv Rev Franç Hematol 12:191–200
5. Tangheroni W, Zorcolo G, Gallo E, Lehmann H (1969) Haemoglobin J Sardegna: α 50 (CD 8) histidine»aspartic acid. Nature 218:470–471