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"); document.write("
Krey-Grauert,\ I.*\ ; Ferro,\ I.F.\ ; Wagner,\ M.
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Antisense oligonucleotide therapies for monogenic disorders.
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Med. Genet. 37, 179-187 (2025)
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Florian,\ K.*\ ; Benet-Pages,\ A.\ ; Berner,\ D.*\ ; Teubert,\ A.*\ ; Eck,\ S.*\ ; Arnold,\ N.*\ ; Bauer,\ P.*\ ; Begemann,\ M.*\ ; Sturm,\ M.*\ ; Kleinle,\ S.*\ ; Haack,\ T.B.*\ ; Eggermann,\ T.*
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Quality assurance within the context of genome diagnostics (a german perspective).
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Med. Genet. 35, 91-104 (2023)
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"); document.write("
Wahida,\ A.\ ; Buschhorn,\ L.*
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Liquid biopsies and those three little words: Finding the perfect match for the MTB.
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Med. Genet. 35, 269-273 (2023)
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Sanin,\ V.*\ ; Schmieder,\ R.*\ ; Ates,\ S.*\ ; Schlieben,\ L.D.\ ; Wiehler,\ J.*\ ; Sun,\ R.*\ ; Decker,\ M.*\ ; Sander,\ M.*\ ; Holdenrieder,\ S.*\ ; Kohlmayer,\ F.*\ ; Friedmann,\ A.*\ ; Mall,\ V.*\ ; Feiler,\ T.*\ ; Dressler,\ A.*\ ; Strom,\ T.M.*\ ; Prokisch,\ H.\ ; Meitinger,\ T.*\ ; von Scheidt,\ M.*\ ; Koenig,\ W.*\ ; Leipold,\ G.*\ ; Schunkert,\ H.*
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Population-based screening in children for early diagnosis and treatment of familial hypercholesterolemia: Design of the VRONI study.
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Med. Genet. 34, 41-51 (2022)
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Prokisch,\ H.
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Molecular diagnostics of Mendelian disorders via combined DNA and RNA sequencing.
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Med. Genet. 31, 191-197 (2019)
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Prokisch,\ H.\ ; Sperl,\ W.*\ ; Meitinger,\ T.\ ; Mayr,\ J.A.*
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Mitochondriopathien \– neue Trends in Diagnostik und Therapie.
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Med. Genet. 27, 282-287 (2015)
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Bettecken,\ T.*\ ; Pfeufer,\ A.\ ; Sudbrak,\ R.*\ ; Siddiqui,\ R.*\ ; Franke,\ A.*\ ; Wienker,\ T.F.*\ ; Krawczak,\ M.*
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Next Generation Sequencing in der diagnostischen Praxis.
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Med. Genet. 26, 21-27 (2014)
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Rogowski,\ W.H.
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Public and Professional Policy Committee der ESHG: Aktivit\äten zur Priorisierung genetischer Tests.
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Med. Genet. 26, 48 (2014)
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Prokisch,\ H.\ ; Oexle,\ K.*\ ; Meitinger,\ T.
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Exomdiagnostik ver\ändert die Sicht auf Mitochondriopathien.
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Med. Genet. 24, 183-186 (2012)
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Heid,\ I.M.\ ; Winkler,\ T.W.*\ ; Grassmann,\ F.*\ ; Weber,\ B.H.F.*
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Wie gro\ß sind die kleinen genetischen Risiken?
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Med. Genet. 23, 377-384 (2011)
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Kronenberg,\ F.*\ ; Heid,\ I.M.
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Genetik intermedi\ärer Ph\änotypen.
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Med. Genet. 19, 304-308 (2007)
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Bickeböller,\ H.
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Parametrische und modellfreie Kopplungsanalysen.
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Med. Genet. 12, 400-402 (2000)
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Golla,\ A.
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Familienbasierte Assoziationsstudien.
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Med. Genet. 12, 419-422 (2000)
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Strom,\ T.M.
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Datenbanken in der Molekularbiologie.
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Med. Genet. 12, 407-411 (2000)
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Wjst,\ M.
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Checklisten zu Design, Durchf\ührung und Datenanalyse in der molekularen Epidemiologie.
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Med. Genet. 12, 416-418 (2000)
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Wjst,\ M.
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Gene f\ür Asthma.
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Med. Genet. 12, 443-447 (2000)
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