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Collinson, William Edward [Editor]Die Katharinenlegende der HS II, 143 der Kgl. Bibliothek zu BrüsselClose
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Published in: Germanische Bibliothek / 2 ; 10
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Collinson, William Edward [Author]Spoken English / Hauptwerk - [14. ed.]Close
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Published in: Spoken English ; Hauptwerk
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Collinson, William Edward [Author]Spoken English / Erg.-H - [7. Aufl.]Close
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Published in: Spoken English ; Erg.-H.
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Collinson, William Edward [Author]Contemporary English : a personal speech recordClose
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Collinson, William Edward [Author] ; True, E. Th [Other]; Jespersen, Otto [Other]Spoken English : on the basis of the work of E. Th. True and O. JespersenClose
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Priebsch, Robert [Author]; Collinson, William Edward [Author]The german language - [6. ed., rev.]Close
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Published in: The great languages
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Priebsch, Robert [Author]; Collinson, William Edward [Author]The German language - [3. ed.]Close
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Published in: The great languages
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Collinson, William Edward; Morris, Alice V.Indication: A Study of Demonstratives, Articles, and Other 'Indicaters'View onlineSchließen
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Published in: Language
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Collinson, William Edward; Morris, Alice V.Indication: A Study of Demonstratives, Articles, and Other 'Indicaters'View onlineSchließen
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Published in: Language
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Blok, Lot Snijders; Rousseau, Justine; Twist, Joanna; Ehresmann, Sophie; Takaku, Motoki; Venselaar, Hanka; Rodan, Lance H.; Nowak, Catherine B.; Douglas, Jessica; Swoboda, Kathryn J.; Steeves, Marcie A.; Sahai, Inderneel; Stumpel, Connie T. R. M.; Stegmann, Alexander P. A.; Wheeler, Patricia; Willing, Marcia; Fiala, Elise; Kochhar, Aaina; Gibson, William T.; Cohen, Ana S. A.; Agbahovbe, Ruky; Innes, A. Micheil; Au, P. Y. Billie; Rankin, Julia; [...]Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and languageView onlineSchließen
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Published in: Nature Communications
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Birling, Marie-Christine; Yoshiki, Atsushi; Adams, David J.; Ayabe, Shinya; Beaudet, Arthur L.; Bottomley, Joanna; Bradley, Allan; Brown, Steve D. M.; Bürger, Antje; Bushell, Wendy; Chiani, Francesco; Chin, Hsian-Jean Genie; Christou, Skevoulla; Codner, Gemma F.; DeMayo, Francesco J.; Dickinson, Mary E.; Doe, Brendan; Donahue, Leah Rae; Fray, Martin D.; Gambadoro, Alessia; Gao, Xiang; Gertsenstein, Marina; Gomez-Segura, Alba; Goodwin, Leslie O.; [...]A resource of targeted mutant mouse lines for 5,061 genesView onlineSchließen
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Published in: Nature Genetics
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Snijders Blok, Lot; Rousseau, Justine; Twist, Joanna; Ehresmann, Sophie; Takaku, Motoki; Venselaar, Hanka; Rodan, Lance H.; Nowak, Catherine B.; Douglas, Jessica; Swoboda, Kathryn J.; Steeves, Marcie A.; Sahai, Inderneel; Stumpel, Connie T. R. M.; Stegmann, Alexander P. A.; Wheeler, Patricia; Willing, Marcia; Fiala, Elise; Kochhar, Aaina; Gibson, William T.; Cohen, Ana S. A.; Agbahovbe, Ruky; Innes, A. Micheil; Au, P. Y. Billie; Rankin, Julia; [...]Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and languageView onlineSchließen
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Published in: Nature Communications
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Snijders Blok, Lot; Rousseau, Justine; Twist, Joanna; Ehresmann, Sophie; Takaku, Motoki; Venselaar, Hanka; Rodan, Lance H.; Nowak, Catherine B.; Douglas, Jessica; Swoboda, Kathryn J.; Steeves, Marcie A.; Sahai, Inderneel; Stumpel, Connie T. R. M.; Stegmann, Alexander P. A.; Wheeler, Patricia; Willing, Marcia; Fiala, Elise; Kochhar, Aaina; Gibson, William T.; Cohen, Ana S. A.; Agbahovbe, Ruky; Innes, A. Micheil; Au, P. Y. Billie; Rankin, Julia; [...]CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and languageView onlineSchließen
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Published in: Nature Communications
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Faundes, Víctor; Newman, William G.; Bernardini, Laura; Canham, Natalie; Clayton-Smith, Jill; Dallapiccola, Bruno; Davies, Sally J.; Demos, Michelle K.; Goldman, Amy; Gill, Harinder; Horton, Rachel; Kerr, Bronwyn; Kumar, Dhavendra; Lehman, Anna; McKee, Shane; Morton, Jenny; Parker, Michael J.; Rankin, Julia; Robertson, Lisa; Temple, I. Karen; Banka, Siddharth; Adam, Shelin; du Souich, Christèle; Elliott, Alison M.; [...]Histone Lysine Methylases and Demethylases in the Landscape of Human Developmental DisordersView onlineSchließen
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Published in: The American Journal of Human Genetics
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O’Donnell-Luria, Anne H.; Pais, Lynn S.; Faundes, Víctor; Wood, Jordan C.; Sveden, Abigail; Luria, Victor; Abou Jamra, Rami; Accogli, Andrea; Amburgey, Kimberly; Anderlid, Britt Marie; Azzarello-Burri, Silvia; Basinger, Alice A.; Bianchini, Claudia; Bird, Lynne M.; Buchert, Rebecca; Carre, Wilfrid; Ceulemans, Sophia; Charles, Perrine; Cox, Helen; Culliton, Lisa; Currò, Aurora; Demurger, Florence; Dowling, James J.; Duban-Bedu, Benedicte; [...]Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and EpilepsyView onlineSchließen
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Published in: The American Journal of Human Genetics
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Sadleir, Lynette G.; Mountier, Emily I.; Gill, Deepak; Davis, Suzanne; Joshi, Charuta; DeVile, Catherine; Kurian, Manju A.; Mandelstam, Simone; Wirrell, Elaine; Nickels, Katherine C.; Murali, Hema R.; Carvill, Gemma; Myers, Candace T.; Mefford, Heather C.; Scheffer, Ingrid E.; Bevan, A. Paul; Dixit, Abhijit; Pridham, Abigail; Tivey, Adrian R.; Sarkar, Ajoy; Donaldson, Alan; Fryer, Alan; Sifrim, Alejandro; Henderson, Alex; [...]Not all SCN1A epileptic encephalopathies are Dravet syndrome : Early profound Thr226Met phenotype : Early profound Thr226Met phenotypeView onlineSchließen
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Published in: Neurology
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Gorman, Kathleen M.; Meyer, Esther; Grozeva, Detelina; Spinelli, Egidio; McTague, Amy; Sanchis-Juan, Alba; Carss, Keren J.; Bryant, Emily; Reich, Adi; Schneider, Amy L.; Pressler, Ronit M.; Simpson, Michael A.; Debelle, Geoff D.; Wassmer, Evangeline; Morton, Jenny; Sieciechowicz, Diana; Jan-Kamsteeg, Eric; Paciorkowski, Alex R.; King, Mary D.; Cross, J. Helen; Poduri, Annapurna; Mefford, Heather C.; Scheffer, Ingrid E.; Haack, Tobias B.; [...]Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-DyskinesiaView onlineSchließen
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Published in: The American Journal of Human Genetics