Anzahl der Einträge: 2.
2020
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.
2016
Girisha, Katta Mohan,
Bidchol, Abdul Mueed,
Graul-Neumann, Luitgard,
Gupta, Ashish,
Hehr, Ute,
Lessel, Davor ,
Nader, Sean,
Shah, Hitesh,
Wickert, Julia und
Kutsche, Kerstin
(2016)
Phenotype and genotype in patients with Larsen syndrome: clinical homogeneity and allelic heterogeneity in seven patients.
BMC Medical Genetics 17 (1).
Volltext nicht vorhanden.
Diese Liste wurde erzeugt am Fri Apr 26 18:47:50 2024 CEST.