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Stradella, Alessandro [Author]; Ansaldi, Girardo [Author] ; Müller-Brühl, Helmut [Performer]; Schlick, Barbara [Performer]; Keller, Helen [Performer]; Dalton, Andrew [Performer]; Thompson, Jan [Performer]; Studer, Ulrich [Performer] Tablater Sängergemeinschaft, Capella ClementinaSan Giovanni Battista : [oratorio in due parti a 5 voci, coro di discipuli e cortigiani, concertino e concerto grosso di Abbate Girardo Ansaldi] (2 Schallpl. in Album)Close
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You can manage bookmarks using lists, please log in to your user account for this.Zürich: Ex Libris-Verl., P 1980
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Stradella, Alessandro [Author] ; Schlick, Barbara [Performer]; Keller, Helen [Performer]; Dalton, Andrew [Performer]; Thompson, Jan [Performer]; Studer, Ulrich [Performer]; Müller-Brühl, Helmut [Performer]; Schmid, Marcel [Performer] Tablater Sängergemeinschaft, Capella ClementinaSan Giovanni Battista : szenisches Oratorium in zwei Teilen = Johannes der Täufer (2 Schallpl. in Kassette)Close
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You can manage bookmarks using lists, please log in to your user account for this.Düsseldorf: Pädag. Verl. Schwann, c 1982
Published in: Schwann musica sacra
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Bach, Johann Christian [Other]; Prin, Jean Baptiste [Other]; Albinoni, Tomaso [Other]; Donizetti, Gaetano [Other]; Gresnick, Antoine-Frédéric [Other]; Danzi, Franz [Other]; Babell, William [Other]; Bach, Johann Sebastian [Other]; Händel, Georg Friedrich [Other]; Hertel, Johann Wilhelm [Other]; Sebon, Karl-Bernhard [Performer]; Cartigny, Gérard [Performer]; Sax, Manfred [Performer]; Ritzkowsky, Johannes [Performer]; Bair, Johannes [Performer]; Immer, Friedemann [Performer]; Touvron, Guy [Performer]; Bardach, Nicholas [Performer]; Karius, Wolfgang [Performer]; Müller-Brühl, Helmut [Performer]; Hucke, Helmut [Performer]; Westermann, Hans-Peter [Performer]; Passin, Günther [Performer]; Stárek, Jiří [Performer]; [...] ; Kölner Kammerorchester, Capella Clementina, Rundfunk im Amerikanischen Sektor Berlins Sinfonietta, Orchestre Symphonique de LiègeBläserkonzerte des 18. Jahrhunderts = 18th century wind concertos (3 Schallpl. in Kassette)Close
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You can manage bookmarks using lists, please log in to your user account for this.Düsseldorf: Päd. Verlag Schwann, c 1981
Published in: Unbekannte Kostbarkeiten - Schwann musica mundi
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Vivaldi, Antonio ; Vivaldi, Antonio Komponist Capella ClementinaVIVALDI, A.: Recorder Concertos, RV 104, 441, 444, 445 (Steinmann, Capella Clementina, Müller-Brühl)View onlineClose
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You can manage bookmarks using lists, please log in to your user account for this.Claves Records, 200427
Published in: Claves Records
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Steinmann, Conrad Komponist; Vivaldi, Antonio Komponist ; Capella ClementinaVIVALDI, A.: Recorder Concertos, RV 104, 441, 444, 445 (Steinmann, Capela Clementina, Müller-Brühl)View onlineClose
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You can manage bookmarks using lists, please log in to your user account for this.Claves Records, 141014
Published in: Claves Records
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Sessa, Fausto; Furlan, Daniela; Zampatti, Clementina; Carnevali, Ileana; Franzi, Francesca; Capella, CarloPrognostic factors for ampullary adenocarcinomas: tumor stage, tumor histology, tumor location, immunohistochemistry and microsatellite instabilityView onlineSchließen
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Published in: Virchows Archiv, 451 (2007) 3, Seite 649-657
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Stowell, Robin; Kussmaul; Trimborn; Clementina, Capella; Muller-Bruhl; Telemann; Tartini; Reichardt; KussmaulConcerto in A Minor for Violin, Strings and ContinuoView onlineSchließen
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Published in: The Musical Times, 123 (1982) 1673, Seite 484
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Matalonga, Leslie; Hernández-Ferrer, Carles; Piscia, Davide; Cohen, Enzo; Cuesta, Isabel; Danis, Daniel; Denommé-Pichon, Anne-Sophie; Duffourd, Yannis; Gilissen, Christian; Johari, Mridul; Laurie, Steven; Li, Shuang; Matalonga, Leslie; Nelson, Isabelle; Peters, Sophia; Paramonov, Ida; Prasanth, Sivakumar; Robinson, Peter; Sablauskas, Karolis; Savarese, Marco; Steyaert, Wouter; van der Velde, Joeri K.; Vitobello, Antonio; Schüle, Rebecca; [...]Correction to: Solving patients with rare diseases through programmatic reanalysis of genome-phenome dataView onlineSchließen
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Published in: European Journal of Human Genetics, 29 (2021) 9, Seite 1466-1469
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Matalonga, Leslie; Hernández-Ferrer, Carles; Piscia, Davide; Cohen, Enzo; Cuesta, Isabel; Danis, Daniel; Denommé-Pichon, Anne-Sophie; Duffourd, Yannis; Gilissen, Christian; Johari, Mridul; Laurie, Steven; Li, Shuang; Matalonga, Leslie; Nelson, Isabelle; Peters, Sophia; Paramonov, Ida; Prasanth, Sivakumar; Robinson, Peter; Sablauskas, Karolis; Savarese, Marco; Steyaert, Wouter; van der Velde, Joeri K.; Vitobello, Antonio; Schüle, Rebecca; [...]Solving patients with rare diseases through programmatic reanalysis of genome-phenome dataView onlineSchließen
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Published in: European Journal of Human Genetics, 29 (2021) 9, Seite 1337-1347
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Zurek, Birte; Ellwanger, Kornelia; Vissers, Lisenka E. L. M.; Schüle, Rebecca; Synofzik, Matthis; Töpf, Ana; de Voer, Richarda M.; Laurie, Steven; Matalonga, Leslie; Gilissen, Christian; Ossowski, Stephan; ’t Hoen, Peter A. C.; Vitobello, Antonio; Schulze-Hentrich, Julia M.; Riess, Olaf; Brunner, Han G.; Brookes, Anthony J.; Rath, Ana; Bonne, Gisèle; Gumus, Gulcin; Verloes, Alain; Hoogerbrugge, Nicoline; Evangelista, Teresinha; Harmuth, Tina; [...]Correction to: Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseasesView onlineSchließen
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Published in: European Journal of Human Genetics, 29 (2021) 9, Seite 1459-1461
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Schüle, Rebecca; Timmann, Dagmar; Erasmus, Corrie E.; Reichbauer, Jennifer; Wayand, Melanie; Baets, Jonathan; Balicza, Peter; Chinnery, Patrick; Dürr, Alexandra; Haack, Tobias; Hengel, Holger; Horvath, Rita; Houlden, Henry; Kamsteeg, Erik-Jan; Kamsteeg, Christoph; Lohmann, Katja; Macaya, Alfons; Marcé-Grau, Anna; Maver, Ales; Molnar, Judit; Münchau, Alexander; Peterlin, Borut; Riess, Olaf; Schöls, Ludger; [...]Correction: Solving unsolved rare neurological diseases—a Solve-RD viewpointView onlineSchließen
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Published in: European Journal of Human Genetics, 29 (2021) 9, Seite 1462-1465
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Zurek, Birte; Ellwanger, Kornelia; Vissers, Lisenka E. L. M.; Schüle, Rebecca; Synofzik, Matthis; Töpf, Ana; de Voer, Richarda M.; Laurie, Steven; Matalonga, Leslie; Gilissen, Christian; Ossowski, Stephan; ’t Hoen, Peter A. C.; Vitobello, Antonio; Schulze-Hentrich, Julia M.; Riess, Olaf; Brunner, Han G.; Brookes, Anthony J.; Rath, Ana; Bonne, Gisèle; Gumus, Gulcin; Verloes, Alain; Hoogerbrugge, Nicoline; Evangelista, Teresinha; Harmuth, Tina; [...]Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseasesView onlineSchließen
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Published in: European Journal of Human Genetics, 29 (2021) 9, Seite 1325-1331
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Schüle, Rebecca; Timmann, Dagmar; Erasmus, Corrie E.; Reichbauer, Jennifer; Wayand, Melanie; Baets, Jonathan; Balicza, Peter; Chinnery, Patrick; Dürr, Alexandra; Haack, Tobias; Hengel, Holger; Horvath, Rita; Houlden, Henry; Kamsteeg, Erik-Jan; Kamsteeg, Christoph; Lohmann, Katja; Macaya, Alfons; Marcé-Grau, Anna; Maver, Ales; Molnar, Judit; Münchau, Alexander; Peterlin, Borut; Riess, Olaf; Schöls, Ludger; [...]Solving unsolved rare neurological diseases—a Solve-RD viewpointView onlineSchließen
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Published in: European Journal of Human Genetics, 29 (2021) 9, Seite 1332-1336
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Denommé-Pichon, Anne-Sophie; Matalonga, Leslie; de Boer, Elke; Jackson, Adam; Benetti, Elisa; Banka, Siddharth; Bruel, Ange-Line; Ciolfi, Andrea; Clayton-Smith, Jill; Dallapiccola, Bruno; Duffourd, Yannis; Ellwanger, Kornelia; Fallerini, Chiara; Gilissen, Christian; Graessner, Holm; Haack, Tobias B.; Havlovicova, Marketa; Hoischen, Alexander; Jean-Marçais, Nolwenn; Kleefstra, Tjitske; López-Martín, Estrella; Macek, Milan; Mencarelli, Maria Antonietta; Moutton, Sébastien; [...]A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencingView onlineSchließen
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Published in: Genetics in Medicine, 25 (2023) 4, Seite 100018
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Demidov, German; Yaldiz, Burcu; Garcia-Pelaez, José; de Boer, Elke; Schuermans, Nika; Van de Vondel, Liedewei; Paramonov, Ida; Johansson, Lennart F.; Musacchia, Francesco; Benetti, Elisa; Bullich, Gemma; Sablauskas, Karolis; Beltran, Sergi; Gilissen, Christian; Hoischen, Alexander; Ossowski, Stephan; de Voer, Richarda; Lohmann, Katja; Oliveira, Carla; Topf, Ana; Vissers, Lisenka E. L. M.; Riess, Olaf; Haack, Tobias B.; Graessner, Holm; [...]Comprehensive reanalysis for CNVs in ES data from unsolved rare disease cases results in new diagnosesView onlineSchließen
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Published in: npj Genomic Medicine, 9 (2024) 1
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Johansson, Lennart F; Laurie, Steve; Spalding, Dylan; Gibson, Spencer; Ruvolo, David; Thomas, Coline; Piscia, Davide; de Andrade, Fernanda; Been, Gerieke; Bijlsma, Marieke; Brunner, Han; Cimerman, Sandi; Dizjikan, Farid Yavari; Ellwanger, Kornelia; Fernandez, Marcos; Freeberg, Mallory; van de Geijn, Gert-Jan; Kanninga, Roan; Maddi, Vatsalya; Mehtarizadeh, Mehdi; Neerincx, Pieter; Ossowski, Stephan; Rath, Ana; Roelofs-Prins, Dieuwke; [...]An interconnected data infrastructure to support large-scale rare disease researchView onlineSchließen
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Published in: GigaScience, 13 (2024)
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Jackson, Adam; Lin, Sheng-Jia; Jones, Elizabeth A.; Chandler, Kate E.; Orr, David; Moss, Celia; Haider, Zahra; Ryan, Gavin; Holden, Simon; Harrison, Mike; Burrows, Nigel; Jones, Wendy D.; Loveless, Mary; Petree, Cassidy; Stewart, Helen; Low, Karen; Donnelly, Deirdre; Lovell, Simon; Drosou, Konstantina; Ambrose, J.C.; Arumugam, P.; Bevers, R.; Bleda, M.; Boardman-Pretty, F.; [...]Clinical, genetic, epidemiologic, evolutionary, and functional delineation of TSPEAR-related autosomal recessive ectodermal dysplasia 14View onlineSchließen
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Published in: Human Genetics and Genomics Advances, 4 (2023) 2, Seite 100186
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Yaldiz, Burcu; Kucuk, Erdi; Hampstead, Juliet; Hofste, Tom; Pfundt, Rolph; Corominas Galbany, Jordi; Rinne, Tuula; Yntema, Helger G.; Hoischen, Alexander; Nelen, Marcel; Gilissen, Christian; Riess, Olaf; Haack, Tobias B.; Graessner, Holm; Zurek, Birte; Ellwanger, Kornelia; Ossowski, Stephan; Demidov, German; Sturm, Marc; Schulze-Hentrich, Julia M.; Schüle, Rebecca; Xu, Jishu; Kessler, Christoph; Wayand, Melanie; [...]Twist exome capture allows for lower average sequence coverage in clinical exome sequencingView onlineSchließen
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Published in: Human Genomics, 17 (2023) 1