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Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...Human mutation, 2016-12, Vol.37 (12), p.1318-1328
- Béroud, Christophe
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- Sobol, Hagay
- Stoppa-Lyonnet, Dominique
- Toulas, Christine
- Trautman, Edwin
- Vaur, Dominique
- Vilquin, Paul
- Weymouth, Katelyn S.
- Willis, Alecia
- Eisenberg, Marcia
- Strom, Charles M
2016
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Human mutation, 2023, Vol.2023, p.1-7
2023
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American journal of human genetics, 2021-10, Vol.108 (10), p.1907-1923
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Biallelic AOPEP Loss‐of‐Function Variants Cause Progressive Dystonia with Prominent Limb Involvement
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2022
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European journal of human genetics : EJHG, 2024-04, Vol.32 (8), p.928-937
- Layo-Carris, Dana E
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- Durham, Emily L
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- Pizoli, Carolyn E
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European journal of human genetics : EJHG, 2024-07, Vol.32 (8), p.1032-1032
- Layo-Carris, Dana E.
- Lubin, Emily E.
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- Clark, Kelly J.
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- Angireddy, Rajesh
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- Mendoza-Londono, Roberto
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- Ziats, Catherine
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- Steel, Dora
- Kurian, Manju
- Barwick, Katy
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- Dagli, Aditi I.
- Nowaczyk, M. J. M.
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- Prchalova, Darina
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- Longo, Nicola
- Platzer, Konrad
- Klöckner, Chiara
- Averdunk, Luisa
- Wieczorek, Dagmar
- Krey, Ilona
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- Reis, Andre
- Balci, Tugce
- Simon, Marleen
- Kroes, Hester Y.
- Wiesener, Antje
- Vasileiou, Georgia
- Marinakis, Nikolaos M.
- Veltra, Danai
- Sofocleous, Christalena
- Kosma, Konstantina
- Synodinos, Joanne Traeger
- Voudris, Konstantinos A.
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- Gueguen, Paul
- Derive, Nicolas
- Colin, Estelle
- Battault, Clarisse
- Au, Billie
- Delatycki, Martin
- Wallis, Mathew
- Gallacher, Lyndon
- Majdoub, Fatma
- Smal, Noor
- Weckhuysen, Sarah
- Schoonjans, An-Sofie
- Kooy, R. Frank
- Meuwissen, Marije
- Cocanougher, Benjamin T.
- Taylor, Kathryn
- Pizoli, Carolyn E.
- McDonald, Marie T.
- James, Philip
- Roeder, Elizabeth R.
- Littlejohn, Rebecca
- Borja, Nicholas A.
- Thorson, Willa
- King, Kristine
- Stoeva, Radka
- Suerink, Manon
- Nibbeling, Esther
- Baskin, Stephanie
- Guyader, Gwenaël L. E.
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- Muss, Candace
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JCO precision oncology, 2023-02, Vol.7 (7), p.e2200582
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- Lippe, Charlotte
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- Prescott, Trine E.
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- Busk, Øyvind L.
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The Journal of cell biology, 2015-11, Vol.211 (3), p.517
2015
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The Journal of cell biology, 2015-11, Vol.211 (3), p.517-532
2015
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The Journal of cell biology, 2015-11, Vol.211 (3), p.517-517
2015
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Human mutation, 2016-12, Vol.37 (12), p.1318-1328
- Béroud, Christophe
- Letovsky, Stanley I.
- Braastad, Corey D.
- Caputo, Sandrine M.
- Beaudoux, Olivia
- Bignon, Yves Jean
- Bressac-De Paillerets, Brigitte
- Bronner, Myriam
- Buell, Crystal M.
- Collod-Béroud, Gwenaëlle
- Coulet, Florence
- Derive, Nicolas
- Divincenzo, Christina
- Elzinga, Christopher D.
- Garrec, Céline
- Houdayer, Claude
- Karbassi, Izabela
- Lizard, Sarab
- Love, Angela
- Muller, Danièle
- Nagan, Narasimhan
- Nery, Camille R.
- Rai, Ghadi
- Revillion, Françoise
- Salgado, David
- Sévenet, Nicolas
- Sinilnikova, Olga
- Sobol, Hagay
- Stoppa-Lyonnet, Dominique
- Toulas, Christine
- Trautman, Edwin
- Vaur, Dominique
- Vilquin, Paul
- Weymouth, Katelyn S.
- Willis, Alecia
- Eisenberg, Marcia
- Strom, Charles M
2016
Volltextzugriff (PDF)
American journal of medical genetics. Part A, 2022, Vol.188 (1), p.272-282
- von der Lippe, Charlotte
- Tveten, Kristian
- Prescott, Trine E
- Holla, Øystein L
- Busk, Øyvind L
- Burke, Katherine B
- Sansbury, Francis H
- Baptista, Júlia
- Fry, Andrew E
- Lim, Derek
- Jolles, Stephen
- Evans, Jennifer
- Osio, Deborah
- Macmillan, Carol
- Bruno, Irene
- Faletra, Flavio
- Climent, Salvador
- Urreitzi, Roser
- Hoenicka, Janet
- Palau, Francesc
- Cohen, Ana S A
- Engleman, Kendra
- Zhou, Dihong
- Amudhavalli, Shivarajan M
- Jeanne, Médéric
- Bonnet-Brilhault, Frédérique
- Lévy, Jonathan
- Drunat, Séverine
- Derive, Nicolas
- Haug, Marte G
- Thorstensen, Wenche M
2022
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Cell reports (Cambridge), 2024-02, Vol.43 (2), p.113773-113773, Article 113773
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Homme, 2017
2017
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