يعرض 1 - 10 نتائج من 24 نتيجة بحث عن '"Paraganglioma genetics"', وقت الاستعلام: 1.83s تنقيح النتائج
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    رسالة جامعية

    المؤلفون: Welander, Jenny

    المساهمون: Linköpings universitet. Institutionen för klinisk och experimentell medicin

    Degree: Diss. (sammanfattning) Linköping : Linköpings universitet, 2015

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    المساهمون: Otolaryngology / Head & Neck Surgery, APH - Quality of Care, Obstetrics and gynaecology, CCA - Cancer biology and immunology, Amsterdam Reproduction & Development (AR&D), Pathology, Guided Treatment in Optimal Selected Cancer Patients (GUTS), Medical Genetics

    المصدر: Oncotarget, 8(9), 14525-14536. Impact Journals
    Oncotarget, 8(9), 14525-14536. Impact Journals LLC
    Oncotarget, 8, 14525-14536
    Oncotarget
    Hoekstra, A S, Hensen, E F, Jordanova, E S, Korpershoek, E, van der Horst-Schrivers, A N A, Cornelisse, C, Corssmit, E P M, Hes, F J, Jansen, J C, Kunst, H P M, Timmers, H J L M, Bateman, A, Eccles, D, Bovee, J V M G, Devilee, P & Bayley, J-P 2017, ' Loss of maternal chromosome 11 is a signature event in SDHAF2, SDHD, and VHL-related paragangliomas, but less significant in SDHB-related paragangliomas ', Oncotarget, vol. 8, no. 9, pp. 14525-14536 . https://doi.org/10.18632/oncotarget.14649
    Oncotarget, 8, 9, pp. 14525-14536
    Oncotarget, 8(9), 14525-14536

    وصف الملف: application/pdf

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    المساهمون: AGEM - Amsterdam Gastroenterology Endocrinology Metabolism, Endocrinology, AMS - Amsterdam Movement Sciences, CCA - Cancer biology and immunology, Otolaryngology / Head & Neck Surgery, Epidemiology and Data Science, APH - Quality of Care, Amsterdam Gastroenterology Endocrinology Metabolism, Guided Treatment in Optimal Selected Cancer Patients (GUTS), Erasmus MC other, Clinical Genetics, Faculty of Physical Education and Physical Therapy, Clinical sciences, Faculty of Law and Criminology

    المصدر: Rijken, J A, Niemeijer, N D, Jonker, M A, Eijkelenkamp, K, Jansen, J C, van Berkel, A, Timmers, H J L M, Kunst, H P M, Bisschop, P H L T, Kerstens, M N, Dreijerink, K M A, van Dooren, M F, van der Horst-Schrivers, A N A, Hes, F J, Leemans, C R, Corssmit, E P M & Hensen, E F 2018, ' The penetrance of paraganglioma and pheochromocytoma in SDHB germline mutation carriers ', Clinical Genetics, vol. 93, no. 1, pp. 60-66 . https://doi.org/10.1111/cge.13055
    Clinical genetics, 93(1), 60-66. Wiley-Blackwell
    Clinical Genetics, 93(1), 60-66. Wiley-Blackwell
    Clinical Genetics, 93, 1, pp. 60-66
    Clinical Genetics, 93(1), 60-66. Wiley
    Clinical Genetics, 93(1), 60-66
    Clinical Genetics, 93(1), 60-66. Wiley-Blackwell Publishing Ltd
    Clinical Genetics, 93, 60-66

    وصف الملف: application/pdf

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    المساهمون: Medical Genetics

    المصدر: Human Molecular Genetics, 25(17), 3715-3728

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