Works matching IS 17558166 AND DT 2015 AND VI 8

Results: 112
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    Rare double-hit with two translocations involving IGH both, with BCL2 and BCL3, in a monoclonal B-cell lymphoma/leukemia.

    Published in:
    Molecular Cytogenetics (17558166), 2015, v. 8, p. 101, doi. 10.1186/s13039-015-0203-y
    By:
    • Alpatov, Roman;
    • Carstens, Billie;
    • Harding, Kimberly;
    • Jarrett, Carolyn;
    • Balakhani, Sudabeh;
    • Lincoln, Jessica;
    • Brzeskiewicz, Peter;
    • Yu Guo;
    • Ohene-Mobley, Alex;
    • LeRoux, Jamie;
    • McDaniel, Veronica;
    • Meltesen, Lynne;
    • Minka, Diane;
    • Patel, Mahendra;
    • Manavi, Cyrus;
    • Swisshelm, Karen
    Publication type:
    Article
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    Copy number variants prioritization after array-CGH analysis – a cohort of 1000 patients.

    Published in:
    Molecular Cytogenetics (17558166), 2015, v. 8, p. 103, doi. 10.1186/s13039-015-0202-z
    By:
    • Carreira, Isabel Marques;
    • Ferreira, Susana Isabel;
    • Matoso, Eunice;
    • Pires, Luís Miguel;
    • Ferrão, José;
    • Jardim, Ana;
    • Mascarenhas, Alexandra;
    • Pinto, Marta;
    • Lavoura, Nuno;
    • Pais, Cláudia;
    • Paiva, Patrícia;
    • Simões, Lúcia;
    • Caramelo, Francisco;
    • Ramos, Lina;
    • Venâncio, Margarida;
    • Ramos, Fabiana;
    • Beleza, Ana;
    • Sá, Joaquim;
    • Saraiva, Jorge;
    • de Melo, Joana Barbosa
    Publication type:
    Article
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    Segmental paleotetraploidy revealed in sterlet (Acipenser ruthenus) genome by chromosome painting.

    Published in:
    Molecular Cytogenetics (17558166), 2015, v. 8, p. 1, doi. 10.1186/s13039-015-0194-8
    By:
    • Romanenko, Svetlana A.;
    • Biltueva, Larisa S.;
    • Serdyukova, Natalya A.;
    • Kulemzina, Anastasia I.;
    • Beklemisheva, Violetta R.;
    • Gladkikh, Olga L.;
    • Lemskaya, Natalia A.;
    • Interesova, Elena A.;
    • Korentovich, Marina A.;
    • Vorobieva, Nadezhda V.;
    • Graphodatsky, Alexander S.;
    • Trifonov, Vladimir A.
    Publication type:
    Article
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    Microdeletions in 9q33.3-q34.11 in five patients with intellectual disability, microcephaly, and seizures of incomplete penetrance: is STXBP1 not the only causative gene?

    Published in:
    Molecular Cytogenetics (17558166), 2015, v. 8, n. 1, p. 1, doi. 10.1186/s13039-015-0178-8
    By:
    • Ehret, Julia K.;
    • Engels, Hartmut;
    • Cremer, Kirsten;
    • Becker, Jessica;
    • Zimmermann, Johannes P.;
    • Wohlleber, Eva;
    • Grasshoff, Ute;
    • Rossier, Eva;
    • Bonin, Michael;
    • Mangold, Elisabeth;
    • Bevot, Andrea;
    • Schön, Stefanie;
    • Heilmann-Heimbach, Stefanie;
    • Dennert, Nicola;
    • Mathieu-Dramard, Michèle;
    • Lacaze, Elodie;
    • Plessis, Ghislaine;
    • de Broca, Alain;
    • Jedraszak, Guillaume;
    • Röthlisberger, Benno
    Publication type:
    Article
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    Cytogenetic and molecular characterization of a recombinant X chromosome in a family with a severe neurologic phenotype and macular degeneration.

    Published in:
    Molecular Cytogenetics (17558166), 2015, v. 8, n. 1, p. 1, doi. 10.1186/s13039-015-0164-1
    By:
    • Magini, Pamela;
    • Poscente, Monica;
    • Ferrari, Simona;
    • Vargiolu, Manuela;
    • Bacchelli, Elena;
    • Graziano, Claudio;
    • Wischmeijer, Anita;
    • Turchetti, Daniela;
    • Malaspina, Elisabetta;
    • Marchiani, Valentina;
    • Cordelli, Duccio Maria;
    • Franzoni, Emilio;
    • Romeo, Giovanni;
    • Seri, Marco
    Publication type:
    Article
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