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Keck, Christoph [Editor]; Auber, Bernd [Other]

Kinderwunschbehandlung in der gynäkologischen Praxis : sinnvolle Diagnostik- und Therapiestrategien für Frauenärzte

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Stuttgart [u.a.]: Thieme, 2014
Mozart, Wolfgang Amadeus [Composer]; Nicolai, Otto [Composer]; Weber, Carl Maria von [Composer]; Donizetti, Gaetano [Composer]; Rossini, Gioachino [Composer]; Auber, Daniel-François-Esprit [Composer]; Mascagni, Pietro [Composer]; Verdi, Giuseppe [Composer] ; Beilke, Irma [Singer]; Rother, Artur [Conductor]; Steiner, Heinrich [Conductor]; Strienz, Wilhelm [Singer]; Schilp, Marie-Luise [Singer]; Trötschel, Elfride [Singer]; Kempe, Rudolf [Conductor]; Aldenhoff, Bernd [Singer]; Weber, Hilmar [Conductor]; Wocke, Hans [Singer]; Ludwig, Walther [Singer]; Steinkopf, Hans [Conductor]; Blumer, Theodor [Conductor]; Hopf, Hans [Singer]; Elmendorff, Karl [Conductor]; Fehenberger, Lorenz [Singer]; Böhme, Kurt [Singer]; Wessely, Karl [Singer]; Scheppan, Hilde [Singer]; Reinecke, Paul [Singer] Rundfunk-Sinfonieorchester Berlin, Reichssender Berlin Orchester, Staatskapelle Dresden, Reichssender Leipzig Chor, ReichssenderLeipzig Großes Orchester, Leipziger Sinfonie-Orchester, Sächsische Staatskapelle Dresden, Deutsches Opernhaus Berlin Orchester

Irma Beilke, Sopran (2 Schallplatten)

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Germany: BASF, [1976]
Melidis, Damianos P. [Author]; Landgraf, Christian [Author]; Schmidt, Gunnar [Author]; Schöner-Heinisch, Anja [Author]; Hardenberg, Sandra von [Author]; Lesinski-Schiedat, Anke [Author]; Nejdl, Wolfgang [Author]; Auber, Bernd [Author]

GenOtoScope: Towards automating ACMG classification of variants associated with congenital hearing loss

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Hannover: Gottfried Wilhelm Leibniz Universität Hannover, 2022 ; Hannover: Technische Informationsbibliothek (TIB), 2022

Published in: PLoS Computational Biology ; 18 (2022), Nr. 9, e1009785
Melidis, Damianos P. [Author]; Landgraf, Christian [Author]; Schmidt, Gunnar [Author]; Schöner-Heinisch, Anja [Author]; Hardenberg, Sandra von [Author]; Lesinski-Schiedat, Anke [Author]; Nejdl, Wolfgang [Author]; Auber, Bernd [Author]

GenOtoScope: Towards automating ACMG classification of variants associated with congenital hearing loss - [published Version]

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San Francisco, Calif. : Public Library of Science, 2022

Published in: PLoS Computational Biology 18 (2022), Nr. 9 ; PLoS Computational Biology
Poker, Yvonne [Author]; Hardenberg, Sandra von [Author]; Hofmann, Winfried [Author]; Tang, Ming [Author]; Baumann, Ulrich [Author]; Schwerk, Nicolaus [Author]; Wetzke, Martin [Author]; Lindenthal, Viola [Author]; Auber, Bernd [Author]; Schlegelberger, Brigitte [Author]; Ott, Hagen [Author]; von Bismarck, Philipp [Author]; Viemann, Dorothee [Author]; Dressler, Frank [Author]; Klemann, Christian [Author]; Bergmann, Anke Katharina [Author]

Systematic genetic analysis of pediatric patients with autoinflammatory diseases

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Hannover: Gottfried Wilhelm Leibniz Universität Hannover, 2023 ; Hannover: Technische Informationsbibliothek (TIB), 2023

Published in: Frontiers in Genetics ; 14 (2023), 1065907
Poker, Yvonne [Author]; Hardenberg, Sandra von [Author]; Hofmann, Winfried [Author]; Tang, Ming [Author]; Baumann, Ulrich [Author]; Schwerk, Nicolaus [Author]; Wetzke, Martin [Author]; Lindenthal, Viola [Author]; Auber, Bernd [Author]; Schlegelberger, Brigitte [Author]; Ott, Hagen [Author]; Bismarck, Philipp von [Author]; Viemann, Dorothee [Author]; Dressler, Frank [Author]; Klemann, Christian [Author]; Bergmann, Anke K. [Author]

Systematic genetic analysis of pediatric patients with autoinflammatory diseases

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2023

Published in: Frontiers in genetics ; 14(2023), Artikel-ID 1065907, Seite 1-11
Poker, Yvonne [Author]; Hardenberg, Sandra von [Author]; Hofmann, Winfried [Author]; Tang, Ming [Author]; Baumann, Ulrich [Author]; Schwerk, Nicolaus [Author]; Wetzke, Martin [Author]; Lindenthal, Viola [Author]; Auber, Bernd [Author]; Schlegelberger, Brigitte [Author]; Ott, Hagen [Author]; von Bismarck, Philipp [Author]; Viemann, Dorothee [Author]; Dressler, Frank [Author]; Klemann, Christian [Author]; Bergmann, Anke Katharina [Author]

Systematic genetic analysis of pediatric patients with autoinflammatory diseases - [published Version]

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Lausanne : Frontiers Media, 2023

Published in: Frontiers in Genetics 14 (2023) ; Frontiers in Genetics
Sepahi, Ilnaz [Author]; Faust, Ulrike [Author]; Sturm, Marc [Author]; Bosse, Kristin [Author]; Kehrer, Martin [Author]; Heinrich, Tilman [Author]; Grundman-Hauser, Kathrin [Author]; Bauer, Peter [Author]; Ossowski, Stephan [Author]; Susak, Hana [Author]; Varon, Raymonda [Author]; Schröck, Evelin [Author]; Niederacher, Dieter [Author]; Auber, Bernd [Author]; Sutter, Christian [Author]; Nguyen, Huu Phuc [Author]

Investigating the effects of additional truncating variants in DNA-repair genes on breast cancer risk in BRCA1-positive women

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London: BioMed Central ; Springer, 2019 ; Heidelberg: Universitätsbibliothek Heidelberg, 2019
v. Hardenberg, Sandra; Klemann, Christian; Auber, Bernd; Baumann, Ulrich

Erratum zu: Warnzeichen für und moderne Diagnostik von angeborenen Störungen des Immunsystems

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Springer Science and Business Media LLC, 2022

Published in: Monatsschrift Kinderheilkunde, 170 (2022) 4, Seite 327-327
v. Hardenberg, Sandra; Klemann, Christian; Auber, Bernd; Baumann, Ulrich

Warnzeichen für und moderne Diagnostik von angeborenen Störungen des Immunsystems

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Springer Science and Business Media LLC, 2022

Published in: Monatsschrift Kinderheilkunde, 170 (2022) 4, Seite 310-326
Wulfmeyer, Vera C.; Auber, Bernd; Haller, Hermann; Schmitt, Roland

Comparison of Different Selection Strategies for Tolvaptan Eligibility among Autosomal Dominant Polycystic Kidney Disease Patients

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S. Karger AG, 2019

Published in: American Journal of Nephrology, 50 (2019) 4, Seite 281-290
Schöne-Bake, Jan-Christoph; Auber, Bernd; Jack, Thomas; Hartmann, Hans

P 411. GNAO1-Associated Hyperkinetic-Dystonic Movement Disorder and Developmental Delay in a 14-Year-Old Girl

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Georg Thieme Verlag KG, 2018

Published in: Abstracts of the 44th Annual Meeting of the Society for Neuropediatrics (2018)
Jülich, Kristina; Horn, Denise; Burfeind, Peter; Erler, Thomas; Auber, Bernd

A Novel MECP2 Mutation in a Boy with Neonatal Encephalopathy and Facial Dysmorphism

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Elsevier BV, 2009

Published in: The Journal of Pediatrics, 155 (2009) 1, Seite 140-143
von Hardenberg, Sandra; Klefenz, Isabel; Steinemann, Doris; Di Donato, Nataliya; Baumann, Ulrich; Auber, Bernd; Klemann, Christian

Current genetic diagnostics in inborn errors of immunity

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Frontiers Media SA, 2024

Published in: Frontiers in Pediatrics, 12 (2024)
Bachmann, Nadine; Auber, Bernd; Das, Anibh; Distelmaier, Felix; Gabriel, Heinz; Himmelreich, Nastassja; Lemke, Johannes; Bergmann, Carsten

Differenzierte Herangehensweise und Testung seltener genetischer Erkrankungen im Kindes- und Jugendalter Differentiated approach and testing for rare genetic diseases in childhood and adolescence

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Springer Science and Business Media LLC, 2024

Published in: Monatsschrift Kinderheilkunde, 172 (2024) 7, Seite 587-594
von Hardenberg, Sandra; Wallaschek, Hannah; Du, Chen; Schmidt, Gunnar; Auber, Bernd

A holistic approach to maximise diagnostic output in trio exome sequencing

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Frontiers Media SA, 2023

Published in: Frontiers in Pediatrics, 11 (2023)
Haake, Kathrin; Wüstefeld, Tim; Merkert, Sylvia; Lüttge, Doreen; Göhring, Gudrun; Auber, Bernd; Baumann, Ulrich; Lachmann, Nico

Human STAT1 gain-of-function iPSC line from a patient suffering from chronic mucocutaneous candidiasis

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Elsevier BV, 2020

Published in: Stem Cell Research, 43 (2020), Seite 101713
Morlot, Susanne; Auber, Bernd; Hille-Betz, Ursula; Pertschy, Stefanie; Steinemann, Doris; Schlegelberger, Brigitte

Consider Family History

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Deutscher Arzte-Verlag GmbH, 2014

Published in: Deutsches Ärzteblatt international (2014)
Stettner, Georg M.; Shoukier, Moneef; Höger, Christoph; Brockmann, Knut; Auber, Bernd

Familial intellectual disability and autistic behavior caused by a small FMR2 gene deletion

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Wiley, 2011

Published in: American Journal of Medical Genetics Part A, 155 (2011) 8, Seite 2003-2007
Brockmann, Knut; Backes, Heiko; Auber, Bernd; Kriebel, Thomas; Stellmer, Franziska; Zoll, Barbara

Overlap of Moebius and oromandibular limb hypogenesis syndrome with gastroschisis and pulmonary hypoplasia

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Wiley, 2009

Published in: American Journal of Medical Genetics Part A, 149A (2009) 12, Seite 2832-2837

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