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Title: [Abnormal hemoglobins identified in Martinique]. Author: Monplaisir N, Galacteros F, Arous N, Rhoda MD, Delanoe-Garin J, Ouka-Montjean M, de Linval JC, Rosa J. Journal: Nouv Rev Fr Hematol (1978); 1985; 27(1):11-4. PubMed ID: 3991355. Abstract: Epidemiologic programs in Martinique during the last 10 years and particularly the last 5, have allowed the determination of the Hb S, Hb C, beta thalassemia traits frequencies. A number of rare variants have been detected during the course of these screening programs. Many of these Hb variants have been analysed at the structural level. For some of them a pathologic interaction with Hb S is observed (Hb D Punjab, Hb O Arab...), and the use of electrophoretic mobilities obtained with the reference samples provides the basis of a rapid, highly probable presumptive identification and then, a useful tool, when for example genetic counselling is necessary.[Abstract] [Full Text] [Related] [New Search]