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1
المؤلفون: Beate Dika, Jan Dreßler, Jeanett Edelmann, Michael Kohl
المصدر: Rechtsmedizin. 32:241-248
مصطلحات موضوعية: Pathology and Forensic Medicine
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::330c61a95c5fa253ff0d0caf943c5e8dTest
https://doi.org/10.1007/s00194-021-00543-zTest -
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المؤلفون: Saskia Hell, Madlen Jentzsch, Georg-Nikolaus Franke, Nadja Jäkel, Susann Schulze, Jeanett Edelmann, Kolja Nenoff, Nora Grieb, Veljko Jeremic, Michael Cross, Sabine Leiblein, Enrica Bach, Wolfram Pönisch, Haifa-Kathrin Al-Ali, Sebastian Schwind, Uwe Platzbecker, Thoralf Lange, Dietger Niederwieser, Vladan Vucinic
المصدر: Bone Marrow Transplantation. 57:824-826
مصطلحات موضوعية: Transplantation, Hematology
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::d34e34af9e64c8e47ca757729d14bdccTest
https://doi.org/10.1038/s41409-022-01609-6Test -
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المؤلفون: M. Kohl, J. Dressler, A. Senst, Jeanett Edelmann
المصدر: Rechtsmedizin. 29:94-100
مصطلحات موضوعية: business.industry, Medicine, business, Molecular biology, Pathology and Forensic Medicine
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::19cc26bdf42f5c462d1188d63e226a98Test
https://doi.org/10.1007/s00194-018-0294-yTest -
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المؤلفون: Anna Klimova, Jeanett Edelmann, Sandra Hering
المصدر: International Journal of Legal Medicine. 134:2061-2062
مصطلحات موضوعية: Male, Linkage disequilibrium, Genetic Linkage, Polymerase Chain Reaction, 01 natural sciences, Hexaplex, Linkage Disequilibrium, Pathology and Forensic Medicine, German, Set (abstract data type), 03 medical and health sciences, 0302 clinical medicine, Germany, Databases, Genetic, Kinship, Humans, 030216 legal & forensic medicine, X chromosome, computer.programming_language, Chromosomes, Human, X, Argus, biology, 010401 analytical chemistry, Haplotype, social sciences, biology.organism_classification, humanities, language.human_language, 0104 chemical sciences, Genetics, Population, Haplotypes, Evolutionary biology, language, computer, Microsatellite Repeats
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::041a96a239d6de34e65519ee0f5e26b4Test
https://doi.org/10.1007/s00414-020-02306-zTest -
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المؤلفون: Carsten Babian, Benjamin Ondruschka, R. Harder, Jeanett Edelmann, Jan Dreßler
المصدر: Rechtsmedizin. 27:43-50
مصطلحات موضوعية: 03 medical and health sciences, 0302 clinical medicine, media_common.quotation_subject, 010401 analytical chemistry, 030216 legal & forensic medicine, Art, Famous persons, 01 natural sciences, Humanities, 0104 chemical sciences, Pathology and Forensic Medicine, media_common
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::16360eeed85e71849f5066dc67162f5bTest
https://doi.org/10.1007/s00194-016-0135-9Test -
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المؤلفون: Jeanett Edelmann, M Nastainczyk-Wulf, Tadeusz Dobosz, M Kawecka-Negrusz, M Sobieszczanska, Jan Dreßler
المصدر: International Journal of Legal Medicine. 131:333-338
مصطلحات موضوعية: ERG1 Potassium Channel, Heterozygote, congenital, hereditary, and neonatal diseases and abnormalities, medicine.medical_specialty, Long QT syndrome, DNA Mutational Analysis, Single-nucleotide polymorphism, 030204 cardiovascular system & hematology, Biology, Polymorphism, Single Nucleotide, QT interval, NAV1.5 Voltage-Gated Sodium Channel, Pathology and Forensic Medicine, Sudden cardiac death, 03 medical and health sciences, 0302 clinical medicine, Internal medicine, Multiplex polymerase chain reaction, medicine, Humans, cardiovascular diseases, 030216 legal & forensic medicine, Genetics, Cardiac arrhythmia, Heterozygote advantage, medicine.disease, Long QT Syndrome, KCNQ1 Potassium Channel, cardiovascular system, Cardiology, Mutation testing, Multiplex Polymerase Chain Reaction
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e6773bf83781b2bf3a4ff85f0af156aTest
https://doi.org/10.1007/s00414-016-1446-9Test -
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المؤلفون: C. Schönefeldt, Jeanett Edelmann, Sandra Hering, Christa Augustin
المصدر: Rechtsmedizin. 26:273-278
مصطلحات موضوعية: 0301 basic medicine, Gynecology, 03 medical and health sciences, medicine.medical_specialty, 030104 developmental biology, 0302 clinical medicine, business.industry, Medicine, 030216 legal & forensic medicine, business, Pathology and Forensic Medicine
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::8612ead8bfbb4314da8b4b32e59f87feTest
https://doi.org/10.1007/s00194-016-0093-2Test -
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المؤلفون: N. Friedewald, J. Bruchhaus, M. Harthun, A.-M. Pflugbeil, K. Thiele, H. Bruchhaus, Jeanett Edelmann, Dirk Labudde
المصدر: Rechtsmedizin. 25:287-293
مصطلحات موضوعية: media_common.quotation_subject, Art, Humanities, Pathology and Forensic Medicine, media_common
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::4c1232208d7c899aeb72b804e9dc816cTest
https://doi.org/10.1007/s00194-015-0043-4Test -
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المؤلفون: Jan Dressler, Andre Hoffmann, M. Kohl, Jeanett Edelmann
المصدر: International Journal of Legal Medicine. 130:357-360
مصطلحات موضوعية: Baltic States, Genetic Markers, Male, 0301 basic medicine, Population, Biology, Pathology and Forensic Medicine, 03 medical and health sciences, 0302 clinical medicine, Gene Frequency, INDEL Mutation, Germany, Multiplex polymerase chain reaction, Humans, 030216 legal & forensic medicine, Indel, education, Allele frequency, X chromosome, Genetic association, Genetics, Chromosomes, Human, X, education.field_of_study, Haplotype, Electrophoresis, Capillary, Amplicon, Genetics, Population, 030104 developmental biology, Female, Multiplex Polymerase Chain Reaction
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3fe00a3eb42d562a1fe92555a53215c4Test
https://doi.org/10.1007/s00414-015-1221-3Test -
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المؤلفون: Sandra Hering, N. Grasern, Jeanett Edelmann, S. Haas
المصدر: Forensic Science International: Genetics Supplement Series. 5:e341-e343
مصطلحات موضوعية: Linkage (software), Genetics, Daughter, Mutation rate, Biological Father, media_common.quotation_subject, Haplotype, Biology, Pathology and Forensic Medicine, Mutation (genetic algorithm), Rare events, Allele, media_common
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::92e93d6108492693376af1531a432b60Test
https://doi.org/10.1016/j.fsigss.2015.09.135Test