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Lloyd Webber, Andrew [Author] ; Brightman, Sarah [Performer]; Richard, Cliff [Performer]; Harley, Steve [Performer]; Miles-Kingston, Paul [Performer]; Lancelot, James [Performer] Winchester Cathedral ChoirAndrew Lloyd Webber's Video Quartet (1 Videokassette)Close
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You can manage bookmarks using lists, please log in to your user account for this.S.l: Really Useful Group, c 1988
Published in: Artwork- Polygram Music Video
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Lloyd Webber, Andrew [Author] ; Maazel, Lorin [Performer]; Domingo, Plácido [Performer]; Brightman, Sarah [Performer]; Miles-Kingston, Paul [Performer]; Neary, Martin [Performer]; Lancelot, James [Performer] Winchester Cathedral Choir, English Chamber OrchestraRequiem (1 Schallpl)Close
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You can manage bookmarks using lists, please log in to your user account for this.Köln: EMI-Electrola, ℗ 1985
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Lloyd Webber, Andrew [Author] ; Domingo, Plácido [Performer]; Brightman, Sarah [Performer]; Miles-Kingston, Paul [Performer]; Neary, Martin [Performer]; Lancelot, James [Performer]; Maazel, Lorin [Performer] Winchester Cathedral Choir, English Chamber OrchestraRequiem (1 CD)Close
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You can manage bookmarks using lists, please log in to your user account for this.Köln: EMI-Electrola, c 1985
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Lloyd Webber, Andrew [Author] ; Domingo, Plácido [Performer]; Brightman, Sarah [Performer]; Miles-Kingston, Paul [Performer]; Neary, Martin [Performer]; Lancelot, James [Performer]; Maazel, Lorin [Performer] Winchester Cathedral Choir, English Chamber OrchestraRequiem (1 CD)Close
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You can manage bookmarks using lists, please log in to your user account for this.Köln: Decca, P 1985
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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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You can manage bookmarks using lists, please log in to your user account for this.Springer Science and Business Media LLC, 2019
Published in: Nature Communications, 10 (2019) 1
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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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You can manage bookmarks using lists, please log in to your user account for this.Springer Science and Business Media LLC, 2019
Published in: Nature Communications, 10 (2019) 1
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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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You can manage bookmarks using lists, please log in to your user account for this.Elsevier BV, 2019
Published in: The American Journal of Human Genetics, 104 (2019) 6, Seite 1210-1222
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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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You can manage bookmarks using lists, please log in to your user account for this.Springer Science and Business Media LLC, 2018
Published in: Nature Communications, 9 (2018) 1
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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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You can manage bookmarks using lists, please log in to your user account for this.Elsevier BV, 2018
Published in: The American Journal of Human Genetics, 102 (2018) 1, Seite 175-187
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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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You can manage bookmarks using lists, please log in to your user account for this.Ovid Technologies (Wolters Kluwer Health), 2017
Published in: Neurology, 89 (2017) 10, Seite 1035-1042
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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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You can manage bookmarks using lists, please log in to your user account for this.Elsevier BV, 2019
Published in: The American Journal of Human Genetics, 104 (2019) 5, Seite 948-956