Hasil Pencarian - Oumar Samassekou

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  1. 1
    Individual Telomere Lengths in Chronic Myeloid Leukemia

    Individual Telomere Lengths in Chronic Myeloid Leukemia oleh Oumar Samassekou, Aimé Ntwari, Josée Hébert, Ju Yan

    Diterbitkan 2009-11-01
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  2. 2
    Contribution of 1p, 19q, 9p and 10q Automated Analysis by FISH to the Diagnosis and Prognosis of Oligodendroglial Tumors According to WHO 2016 Guidelines.

    Contribution of 1p, 19q, 9p and 10q Automated Analysis by FISH to the Diagnosis and Prognosis of Oligodendroglial Tumors According to WHO 2016 Guidelines. oleh Karine Michaud, Marie de Tayrac, Myreille D'Astous, Céline Duval, Claudie Paquet, Oumar Samassekou, Peter Vincent Gould, Stéphan Saikali

    Diterbitkan 2016-01-01
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  3. 3
    Chromosome Arm-Specific Long Telomeres: A New Clonal Event in Primary Chronic Myelogenous Leukemia Cells

    Chromosome Arm-Specific Long Telomeres: A New Clonal Event in Primary Chronic Myelogenous Leukemia Cells oleh Oumar Samassekou, Huiyu Li, Josée Hébert, Aimé Ntwari, Haixia Wang, Catherine Grenier Cliché, Eric Bouchard, Shiang Huang, Ju Yan

    Diterbitkan 2011-06-01
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  4. 4
    A novel mutation in the GARS gene in a Malian family with Charcot‐Marie‐Tooth disease

    A novel mutation in the GARS gene in a Malian family with Charcot‐Marie‐Tooth disease oleh Abdoulaye Yalcouyé, Seybou H. Diallo, Thomas Coulibaly, Lassana Cissé, Salimata Diallo, Oumar Samassékou, Salimata Diarra, Dramane Coulibaly, Mohamed Keita, Cheick O. Guinto, Kenneth Fischbeck, Guida Landouré, The H3Africa Consortium

    Diterbitkan 2019-07-01
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  5. 5
    Friedreich ataxia in a family from Mali, West Africa/Friedreich ataxia in a Malian family

    Friedreich ataxia in a family from Mali, West Africa/Friedreich ataxia in a Malian family oleh Cheick A. K. Cissé, Lassana Cissé, Hamidou O. Ba, Oumar Samassékou, Assiatou Simaga, Abdoulaye Taméga, Salimata Diarra, Seybou H. Diallo, Thomas Coulibaly, Salimata Diallo, Abdoulaye Yalcouyé, Alassane B. Maiga, Mohamed Keita, Kenneth H. Fischbeck, Sékou F. Traoré, Cheick O. Guinto, Guida Landouré, from the H3Africa Consortium

    Diterbitkan 2021-05-01
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  6. 6
    A novel de novo variant in the RUNX2 gene causes cleidocranial dysplasia in a Malian girl

    A novel de novo variant in the RUNX2 gene causes cleidocranial dysplasia in a Malian girl oleh Lassana Cissé, Abdoulaye Yalcouyé, Kadidia Oumar Touré, Youlouza Coulibaly, Alassane Baneye Maiga, Salia Bamba, Dramane Diallo, Salimata Diarra, Abdoulaye Taméga, Oumou Traoré, Mahamadou Kotioumbé, Moussa Aly Sangaré, Hamidou Oumar Ba, Assiatou Simaga, Fatogoma Issa Koné, Oumar Samassekou, Amadou Koné, Cheick Oumar Guinto, Guida Landouré, the H3Africa consortium

    Diterbitkan 2024-02-01
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  7. 7
    AP2A2 mutation and defective endocytosis in a Malian family with hereditary spastic paraplegia

    AP2A2 mutation and defective endocytosis in a Malian family with hereditary spastic paraplegia oleh Salimata Diarra, Saikat Ghosh, Lassana Cissé, Thomas Coulibaly, Abdoulaye Yalcouyé, George Harmison, Salimata Diallo, Seybou H. Diallo, Oumar Coulibaly, Alice Schindler, Cheick A.K. Cissé, Alassane B. Maiga, Salia Bamba, Oumar Samassekou, Mustafa K. Khokha, Emily K. Mis, Saquib A. Lakhani, Frank X. Donovan, Steve Jacobson, Craig Blackstone, Cheick O. Guinto, Guida Landouré, Juan S. Bonifacino, Kenneth H. Fischbeck, Christopher Grunseich

    Diterbitkan 2024-08-01
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