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Hemoglobin
international journal for hemoglobin research
Volume 14, 1990 - Issue 5
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Original Article

A Simple Approach To the Determination of the γ Chain Composition of F in Adult Human Blood Samples

L. Manca Istituto di Fisiologia Generale e Chimica Biologica Universita di Sassari, 1-07100, Sassari, Italy
&
B. Masaia Istituto di Fisiologia Generale e Chimica Biologica Universita di Sassari, 1-07100, Sassari, Italy
Pages 517-527 | Received 03 Apr 1990, Accepted 30 Aug 1990, Published online: 07 Jul 2009

Citations (7)

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Read on this site (2)

L. Manca, B. Masala, M. Manca, P. Ferranti & P. Pucci. (1994) Hb G-Miwlo [α64(E13)ASP→ASN] Observed in a Caucasian Family. Hemoglobin 18:1, pages 53-56.
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Bruno Masala. (1992) Hemoglobinopathies in Sardinia. Hemoglobin 16:4, pages 331-351.
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Articles from other publishers (5)

Sandro Trova, Paolo Mereu, Elena Cocco, Bruno Masala, Laura Manca & Monica Pirastru. (2016) The New -474(C&#x2192;T) Substitution Discovered in the <b><i>HBG2</i></b> Promoter of a Sardinian δβ-Thalassemia Carrier. Acta Haematologica 136:3, pages 178-185.
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Laura Manca & Bruno Masala. (2008) Disorders of the synthesis of human fetal hemoglobin. IUBMB Life 60:2, pages 94-111.
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Bruno Masala & Laura Manca. 1994. Hemoglobins Part B: Biochemical and Analytical Methods. Hemoglobins Part B: Biochemical and Analytical Methods 21 44 .
Bruno Masala, Laura Manca & Carlo Callegarini. (1992) Symmetric and asymmetric tetramers, due to multiple α- and β-globin chains, account for the hemoglobin polymorphism of the Italian catfish (Ictalurus sp.). Comparative Biochemistry and Physiology Part B: Comparative Biochemistry 102:4, pages 779-783.
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L. Manca, E. Cocco, D. Gallisai, B. Masala & J. G. Gilman. (2008) Diminished A γ T fetal globin levels in Sardinian haplotype II β°‐thalassaemia patients are associated with a four base pair deletion in the A γ T promoter . British Journal of Haematology 78:1, pages 105-107.
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