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1.
Bull Soc Pathol Exot Filiales ; 78(1): 89-93, 1985.
Article in French | MEDLINE | ID: mdl-3986955

ABSTRACT

In November 1983, HB A2 Babinga was found in a Columbian male in Paris. Blood samples from Columbia showed that his mother and one of his brothers were also Hb A2 Babinga carriers and that his mother and another brother and his sister were Hb S carriers.


Subject(s)
Hemoglobin A2/genetics , Hemoglobin A/genetics , Adult , Anemia, Sickle Cell/genetics , Colombia , Electrophoresis, Cellulose Acetate , Genetic Carrier Screening , Hemoglobin A2/analysis , Hemoglobin, Sickle/genetics , Hemoglobinopathies/genetics , Humans , Male
3.
Nouv Rev Fr Hematol (1978) ; 21(4): 353-7, 1979.
Article in French | MEDLINE | ID: mdl-553283

ABSTRACT

Studies on five generations of the Maghrebian family representing two double heterozygous subjects Hb C/Hb O Arab. Review of literature concerning Hb O Arab; identification and screening techniques; historic and genetic implications.


Subject(s)
Hemoglobin C/genetics , Heterozygote , Egypt , Humans , Mutation , Saudi Arabia , Sudan
4.
Nouv Rev Fr Hematol (1978) ; 20(3): 465-77, 1978 Nov 25.
Article in French | MEDLINE | ID: mdl-754177

ABSTRACT

Since 1962, the hemoglobin of all the foundation scholars of the French Cooperation addressed to the C.E.A.B.H. for a medical examination at their arrival in France was systematically studied. The distribution and the incidence of hemoglobin S and hemoglobin C were recorded in fourthy ethnic groups from Africa South of Sahara. Few significant correlations between the frequency of anomalies detected by the medico-biological check-up and the presence of an abnormal hemoglobin were found; AC seems to be less asymptomatic than AS. Some rare hemoglobins were detected.


Subject(s)
Hemoglobins, Abnormal/analysis , Mass Screening , Adult , Africa/ethnology , Fetal Hemoglobin/analysis , France , Hemoglobin A2/analysis , Hemoglobin C/analysis , Hemoglobin E/analysis , Hemoglobin J/analysis , Hemoglobin, Sickle/analysis , Hemoglobins, Abnormal/genetics , Heterozygote , Homozygote , Humans , Male , Thalassemia/epidemiology , Thalassemia/genetics
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