يعرض 1 - 3 نتائج من 3 نتيجة بحث عن '"E. A. Nannenberg"', وقت الاستعلام: 0.68s تنقيح النتائج
  1. 1
    Prenatal Diagnosis and Preimplantation Genetic Testing for Inherited Cardiac Diseases

    المؤلفون: E. A. Nannenberg, Y. Arens

    المساهمون: Human Genetics, ACS - Atherosclerosis & ischemic syndromes, ACS - Amsterdam Cardiovascular Sciences, Human genetics

    المصدر: Clinical Cardiogenetics ISBN: 9783030454562
    Clinical Cardiogenetics: Third Edition, 457-461
    STARTPAGE=457;ENDPAGE=461;TITLE=Clinical Cardiogenetics: Third Edition
    Nannenberg, E A & Arens, Y 2020, Prenatal Diagnosis and Preimplantation Genetic Testing for Inherited Cardiac Diseases . in Clinical Cardiogenetics: Third Edition . Clinical Cardiogenetics: Third Edition, Springer International Publishing, pp. 457-461 . https://doi.org/10.1007/978-3-030-45457-9_27Test

    مصطلحات موضوعية: Assisted reproductive technology, medicine.diagnostic_test, business.industry, medicine.medical_treatment, Genomics, Prenatal diagnosis, Disease, medicine.disease, Bioinformatics, Penetrance, Sudden cardiac death, medicine, Medical diagnosis, business, Genetic testing

    الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c09358c80a427f80cfaf34273e889d53Test
    https://doi.org/10.1007/978-3-030-45457-9_27Test


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  2. 2
    Recurrent and founder mutations in the Netherlands – Phospholamban p.Arg14del mutation causes arrhythmogenic cardiomyopathy*

    المؤلفون: P. A. van der Zwaag, I. A. W. van Rijsingen, R. de Ruiter, E. A. Nannenberg, J. A. Groeneweg, J. G. Post, R. N. W. Hauer, I. C. van Gelder, M. P. van den Berg, P. van der Harst, A. A. M. Wilde, J. P. van Tintelen

    المصدر: De Nederlandse gezondheidszorg ISBN: 9789036807043

    الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::9c3cac4df5e02ff362b8019d40020a2cTest
    https://doi.org/10.1007/978-90-368-0705-0_11Test


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  3. 3
    [Genetic identification of patients and families with a long-QT syndrome: large regional differences in the result of 10 years]

    المؤلفون: N, Hofman, P G, Postema, I M, van Langen, E A, Nannenberg, M, Alders, R, Jongbloed, H J M, Smeets, A A M, Wilde

    المصدر: Nederlands tijdschrift voor geneeskunde. 151(11)

    مصطلحات موضوعية: Cohort Studies, Long QT Syndrome, Genotype, DNA Mutational Analysis, Prevalence, Humans, Genetic Predisposition to Disease, Genetic Testing, Netherlands, Retrospective Studies

    الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::77ad2711097a0fd283c424d3233cf1afTest
    https://pubmed.ncbi.nlm.nih.gov/17441564Test


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