Anzahl der Einträge: 2.
Lessel, Davor ,
Zeitler, Daniela M.,
Reijnders, Margot R. F.,
Kazantsev, Andriy,
Hassani Nia, Fatemeh,
Bartholomäus, Alexander,
Martens, Victoria,
Bruckmann, Astrid,
Graus, Veronika,
McConkie-Rosell, Allyn,
McDonald, Marie,
Lozic, Bernarda,
Tan, Ee-Shien,
Gerkes, Erica,
Johannsen, Jessika,
Denecke, Jonas,
Telegrafi, Aida,
Zonneveld-Huijssoon, Evelien,
Lemmink, Henny H.,
Cham, Breana W. M.,
Kovacevic, Tanja,
Ramsdell, Linda,
Foss, Kimberly,
Le Duc, Diana,
Mitter, Diana,
Syrbe, Steffen,
Merkenschlager, Andreas,
Sinnema, Margje,
Panis, Bianca,
Lazier, Joanna,
Osmond, Matthew,
Hartley, Taila,
Mortreux, Jeremie,
Busa, Tiffany,
Missirian, Chantal,
Prasun, Pankaj,
Lüttgen, Sabine,
Mannucci, Ilaria,
Lessel, Ivana ,
Schob, Claudia,
Kindler, Stefan,
Pappas, John ,
Rabin, Rachel,
Willemsen, Marjolein,
Gardeitchik, Thatjana,
Löhner, Katharina,
Rump, Patrick,
Dias, Kerith-Rae,
Evans, Carey-Anne,
Andrews, Peter Ian,
Roscioli, Tony,
Brunner, Han G.,
Chijiwa, Chieko,
Lewis, M. E. Suzanne ,
Jamra, Rami Abou,
Dyment, David A.,
Boycott, Kym M.,
Stegmann, Alexander P. A.,
Kubisch, Christian,
Tan, Ene-Choo,
Mirzaa, Ghayda M.,
McWalter, Kirsty,
Kleefstra, Tjitske,
Pfundt, Rolph,
Ignatova, Zoya,
Meister, Gunter und
Kreienkamp, Hans-Jürgen
(2020)
Germline AGO2 mutations impair RNA interference and human neurological development.
Nature Communications 11 (1).
Volltext nicht vorhanden.
Neuhaus, Christine,
Eisenberger, Tobias,
Decker, Christian,
Nagl, Sandra,
Blank, Cornelia,
Pfister, Markus,
Kennerknecht, Ingo,
Müller-Hofstede, Cornelie,
Charbel Issa, Peter,
Heller, Raoul,
Beck, Bodo,
Rüther, Klaus,
Mitter, Diana,
Rohrschneider, Klaus,
Steinhauer, Ute,
Korbmacher, Heike M.,
Huhle, Dagmar,
Elsayed, Solaf M.,
Taha, Hesham M.,
Baig, Shahid M.,
Stöhr, Heidi,
Preising, Markus,
Markus, Susanne,
Moeller, Fabian,
Lorenz, Birgit,
Nagel-Wolfrum, Kerstin,
Khan, Arif O. und
Bolz, Hanno J.
(2017)
Next-generation sequencing reveals the mutational landscape of clinically diagnosed Usher syndrome: copy number variations, phenocopies, a predominant target for translational read-through, and PEX26 mutated in Heimler syndrome.
Molecular Genetics & Genomic Medicine 5 (5), S. 531-552.
Volltext nicht vorhanden.
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