Search Results - Oumar Samassekou

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  1. 1

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

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  2. 2

    Acquired pericentric inversion of der(9) with BCR and ABL1 codeletion in chronic myeloid leukemia: a rare cytogenetic finding from Mali by Oumar Samassekou, Modibo K. Goita, Madani Ly, Moussa Bathily, Christine Ongoiba, Guida Landouré, Mahamadou Traoré

    Published in Molecular Cytogenetics (2026-04-01)
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  3. 3

    Down Syndrome due to de Novo Robertsonian Translocation Rob(21;21) in Mali by Christine Ongoiba, Oumar Samassekou, Oumou Traoré, Cheick O. Sidibé, Modibo K. Goita, Guida Landouré, Mahamadou Traoré

    Published in Clinical Case Reports (2026-04-01)
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  4. 4

    Using the Fluorescence In Situ Hybridization in the Diagnosis of Trisomy 13 in a Male Newborn From Mali by Alassane Baneye Maiga, Oumar Samassekou, Cheick Oumar Sidibé, Oumou Traoré, Belco Maiga, Mahamadou Traoré, Cheick Oumar Guinto, Guida Landouré

    Published in Clinical Case Reports (2025-10-01)
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  5. 5

    Using the Fluorescence In Situ Hybridization in the Diagnosis of Trisomy 13 in a Male Newborn From Mali by Alassane Baneye Maiga, Oumar Samassekou, Cheick Oumar Sidibé, Oumou Traoré, Belco Maiga, Mahamadou Traoré, Cheick Oumar Guinto, Guida Landouré

    Published in Clinical Case Reports (2025-10-01)
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  6. 6

    A novel mutation in the GARS gene in a Malian family with Charcot‐Marie‐Tooth disease by 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

    Published in Molecular Genetics & Genomic Medicine (2019-07-01)
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  7. 7

    A novel de novo variant in the RUNX2 gene causes cleidocranial dysplasia in a Malian girl by 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

    Published in Clinical Case Reports (2024-02-01)
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  8. 8

    AP2A2 mutation and defective endocytosis in a Malian family with hereditary spastic paraplegia by 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

    Published in Neurobiology of Disease (2024-08-01)
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