Search Results - Klee, Eric W.

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    The expanding clinical and genetic spectrum of DYNC1H1-related disorders by Möller, Birk (Author) , Becker, Lena-Luise (Author) , Saffari, Afshin (Author) , Afenjar, Alexandra (Author) , Coci, Emanuele (Author) , Williamson, Rachel (Author) , Ward-Melver, Catherine (Author) , Gibaud, Marc (Author) , Sedláčková, Lucie (Author) , Laššuthová, Petra (Author) , Libá, Zuzana (Author) , Vlčková, Markéta (Author) , William, Nancy (Author) , Klee, Eric W (Author) , Gavrilova, Ralitza H (Author) , Lévy, Jonathan (Author) , Capri, Yline (Author) , Scavina, Mena (Author) , Körner, Robert Walter (Author) , Valivullah, Zaheer (Author) , Weiß, Claudia (Author) , Möller, Greta Marit (Author) , Frazier, Zoë (Author) , Roberts, Amy (Author) , Gener, Blanca (Author) , Scala, Marcello (Author) , Striano, Pasquale (Author) , Zara, Federico (Author) , Thiel, Moritz (Author) , Sinnema, Margje (Author) , Kamsteeg, Erik-Jan (Author) , Donkervoort, Sandra (Author) , Duboc, Veronique (Author) , Zaafrane-Khachnaoui, Khaoula (Author) , Elkhateeb, Nour (Author) , Selim, Laila (Author) , Margot, Henri (Author) , Marin, Victor (Author) , Beneteau, Claire (Author) , Isidor, Bertrand (Author) , Cogne, Benjamin (Author) , Keren, Boris (Author) , Küsters, Benno (Author) , Beggs, Alan H (Author) , Sveden, Abigail (Author) , Chopra, Maya (Author) , Genetti, Casie A (Author) , Nicolai, Joost (Author) , Dötsch, Jörg (Author) , Koy, Anne (Author) , Bönnemann, Carsten G (Author) , Hagen, Maja von der (Author) , Kleist-Retzow, Jürgen-Christoph von (Author) , Voermans, Nicol C (Author) , Jungbluth, Heinz (Author) , Dafsari, Hormos Salimi (Author) ,


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    A reverse genetics and genomics approach to gene paralog function and disease: myokymia and the juxtaparanode by Marafi, Dana (Author) , Kozar, Nina (Author) , Duan, Ruizhi (Author) , Bradley, Stephen (Author) , Yokochi, Kenji (Author) , Al Mutairi, Fuad (Author) , Saadi, Nebal Waill (Author) , Whalen, Sandra (Author) , Brunet, Theresa (Author) , Kotzaeridou, Urania (Author) , Choukair, Daniela (Author) , Keren, Boris (Author) , Nava, Caroline (Author) , Kato, Mitsuhiro (Author) , Arai, Hiroshi (Author) , Froukh, Tawfiq (Author) , Faqeih, Eissa Ali (Author) , AlAsmari, Ali M. (Author) , Saleh, Mohammed M. (Author) , Pinto e Vairo, Filippo (Author) , Pichurin, Pavel N. (Author) , Klee, Eric W. (Author) , Schmitz, Christopher T. (Author) , Grochowski, Christopher M. (Author) , Mitani, Tadahiro (Author) , Herman, Isabella (Author) , Calame, Daniel G. (Author) , Fatih, Jawid M. (Author) , Du, Haowei (Author) , Coban-Akdemir, Zeynep (Author) , Pehlivan, Davut (Author) , Jhangiani, Shalini N. (Author) , Gibbs, Richard A. (Author) , Miyatake, Satoko (Author) , Matsumoto, Naomichi (Author) , Wagstaff, Laura J. (Author) , Posey, Jennifer E. (Author) , Lupski, James R. (Author) , Meijer, Dies (Author) , Wagner, Matias (Author) ,


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  3. 3
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    RINT1 bi-allelic variations cause infantile-onset recurrent acute liver failure and skeletal abnormalities by Cousin, Margot (Author) , Conboy, Erin (Author) , Wang, Jian-She (Author) , Lenz, Dominic (Author) , Schwab, Tanya L. (Author) , Williams, Monique (Author) , Abraham, Roshini S. (Author) , Barnett, Sarah (Author) , El-Youssef, Mounif (Author) , Graham, Rondell P. (Author) , Gutierrez Sanchez, Luz Helena (Author) , Hasadsri, Linda (Author) , Hoffmann, Georg F. (Author) , Hull, Nathan C. (Author) , Kopajtich, Robert (Author) , Kovacs-Nagy, Reka (Author) , Li, Jia-qi (Author) , Marx-Berger, Daniela (Author) , McLin, Valérie (Author) , McNiven, Mark A. (Author) , Mounajjed, Taofic (Author) , Prokisch, Holger (Author) , Rymen, Daisy (Author) , Schulze, Ryan J. (Author) , Staufner, Christian (Author) , Yang, Ye (Author) , Clark, Karl J. (Author) , Lanpher, Brendan C. (Author) , Klee, Eric W. (Author) ,


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