Search Results - "Hariti, G"

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  1. 1

    Prevention and treatment of COVID-19-associated hypercoagulability: Recommendations of the Algerian society of transfusion and hemobiology by Chekkal, M., Deba, T., Hadjali, S., Lamara, H., Oulaa, H., Zouai, K., Hariti, G.

    “…Since December 2019, an outbreak of coronavirus disease 2019 (COVID-19) in Wuhan, China, has spread throughout the world. Coagulation dysfunction is one of the…”
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    Journal Article
  2. 2

    Genetic diversity in the Iberian Peninsula determined from mitochondrial sequence analysis by Côrte-Real, H B, Macaulay, V A, Richards, M B, Hariti, G, Issad, M S, Cambon-Thomsen, A, Papiha, S, Bertranpetit, J, Sykes, B C

    Published in Annals of human genetics (01-07-1996)
    “…We have analysed 302 bp of the first hypervariable region of the mitochondrial D-loop in 271 individuals from different regions of the Iberian Peninsula and 85…”
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  3. 3

    Y chromosome STR haplotypes in four populations from northwest Africa by Bosch, E, Calafell, F, Pérez-Lezaun, A, Comas, D, Izaabel, H, Akhayat, O, Sefiani, A, Hariti, G, Dugoujon, J M, Bertranpetit, J

    “…The eight short tandem repeat (STR) polymorphic systems mapping on the male-specific region of the human Y chromosome, DYS19, DYS388, DYS389I, DYS389II,…”
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  4. 4

    Genetic structure of north-west Africa revealed by STR analysis by Bosch, E, Calafell, F, Pérez-Lezaun, A, Clarimón, J, Comas, D, Mateu, E, Martínez-Arias, R, Morera, B, Brakez, Z, Akhayat, O, Sefiani, A, Hariti, G, Cambon-Thomsen, A, Bertranpetit, J

    Published in European journal of human genetics : EJHG (01-05-2000)
    “…We have analysed a large set of autosomal short tandem repeat (STR) loci in several Arabic and Berber-speaking groups from north-west Africa (ie Moroccan…”
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  5. 5

    Absence of the hemochromatosis gene Cys282Tyr mutation in three ethnic groups from Algeria (Mzab), Ethiopia, and Senegal by Roth, M, Giraldo, P, Hariti, G, Poloni, E S, Sanchez-Mazas, A, Stefano, G F, Dugoujon, J M, Coppin, H

    Published in Immunogenetics (New York) (01-01-1997)
    “…A Celtic origin for hemochromatosis, a common genetic iron metabolism disorder, has been postulated for a long time. To check whether the two mutations…”
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    Journal Article
  6. 6