Hasil Pencarian - Irén Haltrich

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  1. 1
    What should we consider in the case of combined Down- and 47,XY,+i(X)(q10) Klinefelter syndromes? The unique case of a male newborn and review of the literature

    What should we consider in the case of combined Down- and 47,XY,+i(X)(q10) Klinefelter syndromes? The unique case of a male newborn and review of the literature oleh Eva Pinti, Anna Lengyel, Gyorgy Fekete, Iren Haltrich

    Diterbitkan 2020-01-01
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  2. 2
    Diagnostic difficulties and possibilities of NF1-like syndromes in childhood

    Diagnostic difficulties and possibilities of NF1-like syndromes in childhood oleh Eva Pinti, Krisztina Nemeth, Krisztina Staub, Anna Lengyel, Gyorgy Fekete, Iren Haltrich

    Diterbitkan 2021-07-01
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  3. 3
    Parallel evolution under chemotherapy pressure in 29 breast cancer cell lines results in dissimilar mechanisms of resistance.

    Parallel evolution under chemotherapy pressure in 29 breast cancer cell lines results in dissimilar mechanisms of resistance. oleh Bálint Tegze, Zoltán Szállási, Irén Haltrich, Zsófia Pénzváltó, Zsuzsa Tóth, István Likó, Balázs Gyorffy

    Diterbitkan 2012-01-01
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  4. 4
    Study of patterns of inheritance of premature ovarian failure syndrome carrying maternal and paternal premutations

    Study of patterns of inheritance of premature ovarian failure syndrome carrying maternal and paternal premutations oleh Artur Beke, Henriett Piko, Iren Haltrich, Veronika Karcagi, Janos Rigo, Maria Judit Molnar, György Fekete

    Diterbitkan 2018-07-01
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  5. 5
    Clinical evaluation of rare copy number variations identified by chromosomal microarray in a Hungarian neurodevelopmental disorder patient cohort

    Clinical evaluation of rare copy number variations identified by chromosomal microarray in a Hungarian neurodevelopmental disorder patient cohort oleh Anna Lengyel, Éva Pinti, Henriett Pikó, Árvai Kristóf, Tünde Abonyi, Zaránd Némethi, György Fekete, Irén Haltrich

    Diterbitkan 2022-11-01
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  6. 6
    Generation of multiple iPSC clones from a male schizophrenia patient carrying de novo mutations in genes KHSRP, LRRC7, and KIR2DL1, and his parents

    Generation of multiple iPSC clones from a male schizophrenia patient carrying de novo mutations in genes KHSRP, LRRC7, and KIR2DL1, and his parents oleh Edit Hathy, Eszter Szabó, Katalin Vincze, Irén Haltrich, Eszter Kiss, Nóra Varga, Zsuzsa Erdei, György Várady, László Homolya, Ágota Apáti, János M. Réthelyi

    Diterbitkan 2021-03-01
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  7. 7
    An Ultra-Rare Manifestation of an X-Linked Recessive Disorder: Duchenne Muscular Dystrophy in a Female Patient

    An Ultra-Rare Manifestation of an X-Linked Recessive Disorder: Duchenne Muscular Dystrophy in a Female Patient oleh Zsuzsanna Szűcs, Éva Pinti, Irén Haltrich, Orsolya Pálné Szén, Tibor Nagy, Endre Barta, Gábor Méhes, László Bidiga, Olga Török, Anikó Ujfalusi, Katalin Koczok, István Balogh

    Diterbitkan 2022-10-01
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  8. 8
    Normal karyotype is a poor prognostic factor in myeloid leukemia of Down syndrome: a retrospective, international study

    Normal karyotype is a poor prognostic factor in myeloid leukemia of Down syndrome: a retrospective, international study oleh Marjolein Blink, Martin Zimmermann, Christine von Neuhoff, Dirk Reinhardt, Valerie de Haas, Henrik Hasle, Maureen M. O’Brien, Batia Stark, Julie Tandonnet, Andrea Pession, Katerina Tousovska, Daniel K.L. Cheuk, Kazuko Kudo, Takashi Taga, Jeffrey E. Rubnitz, Iren Haltrich, Walentyna Balwierz, Rob Pieters, Erik Forestier, Bertil Johansson, Marry M. van den Heuvel-Eibrink, C. Michel Zwaan

    Diterbitkan 2014-02-01
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  9. 9
    PB1699: GENOMIC AND TRANSCRIPTOMIC PROFILING REVEALS NOVEL GENE FUSIONS AND MARKERS OF CLINICAL RESPONSE IN PEDIATRIC ACUTE LYMPHOBLASTIC LEUKEMIA

    PB1699: GENOMIC AND TRANSCRIPTOMIC PROFILING REVEALS NOVEL GENE FUSIONS AND MARKERS OF CLINICAL RESPONSE IN PEDIATRIC ACUTE LYMPHOBLASTIC LEUKEMIA oleh Borbála Péterffy, Szilvia Krizsán, Bálint Egyed, Gábor Bedics, Anna Bekő, Dániel János Erdélyi, Judit Müller, Tibor Nagy, Lajos László Hegyi, Zsuzsanna Jakab, György Péter, Marianna Zombori, Krisztina Csanádi, Gábor Ottóffy, Katalin Csernus, Ágnes Vojcek, Lilla Györgyi Tiszlavicz, Krisztina Míta Gábor, Ágnes Kelemen, Péter Hauser, Krisztián Kállay, Gabriella Kertész, Zsuzsanna Gaál, István Szegedi, Ágnes Márk, Irén Haltrich, Zsuzsanna Hevessy, Anikó Ujfalusi, Béla Kajtár, Csongor Kiss, Gergely Kriván, András Matolcsy, Gábor Kovács, Csaba Bödör, Donát Alpár

    Diterbitkan 2023-08-01
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