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Matthias Begemann

RWTH Aachen University

32H指数
157论文数
3.9K被引数
收录论文 61
发表时间
Author Correction: Diagnosis and management of Silver–Russell syndrome: second international consensus statement作者更正:Silver–Russell综合征的诊断与管理:第二份国际共识声明
err2026-09-30
err0
PREAI
errEmma Wakeling; Justin H. Davies; Eloïse Giabicani; Susan M. O’Connell; Madeleine D. Harbison; Amélie Perriere; Jennifer B. Salem; Matthias Begemann; Gerhard Binder; Frédéric Brioude; Dayna Morris-Carney; Jovanna Dahlgren; Bea Dickinson; Bruno Donadille; Beatrice Dubern; Katja Eggermann; Gabriella Gazdagh; Karen Grønskov; Anita C. Hokken Koelega; Youn Hee Jee; Alicia Jurians; Masayo Kagami; Satomi Koyama; Emilie Kulak; Asmahane Ladjouze; Paola Lombardi; Mohamad Maghnie; Louise McClelland; Veronica Mericq; Giuseppa Patti; Klaudia Raabe; Andrea Riccio; Silvia Russo; Helen L. Storr; I. Karen Temple; Zeynep Tümer; Thomas Eggermann; Deborah J. G. Mackay; Irene Netchine
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Diagnosis and management of Silver–Russell syndrome: second international consensus statement银- Russell 综合征的诊断与管理:第二届国际共识声明
err2026-09-23
err0
PREAI
errEmma Wakeling; Justin H. Davies; Eloïse Giabicani; Susan M. O’Connell; Madeleine D. Harbison; Amélie Perriere; Jennifer B. Salem; Matthias Begemann; Gerhard Binder; Frédéric Brioude; Dayna Morris-Carney; Jovanna Dahlgren; Bea Dickinson; Bruno Donadille; Beatrice Dubern; Katja Eggermann; Gabriella Gazdagh; Karen Grønskov; Anita C. Hokken Koelega; Youn Hee Jee; Alicia Jurians; Masayo Kagami; Satomi Koyama; Emilie Kulak; Asmahane Ladjouze; Paola Lombardi; Mohamad Maghnie; Louise McClelland; Veronica Mericq; Guiseppa Patti; Klaudia Raabe; Andrea Riccio; Silvia Russo; Helen L. Storr; I. Karen Temple; Zeynep Tümer; Thomas Eggermann; Deborah J. G. Mackay; Irene Netchine
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Prenatal Genetic Testing for Beckwith-Wiedemann Syndrome: Considerations, Challenges and Observations (A Real-World Study)产前基因检测在贝克威思-威德曼综合征中的应用:考量、挑战与观察(一项真实世界研究)
err2026-06-25
err0
errOAAI
errMelissa Connolly; Louise McClelland; Pierpaola Tannorella; Tanja Richter; Ester Mainini; Andreas Dufke; Annette Lischka; Matthias Begemann; Katja Eggermann; Thomas Eggermann; Silvia Russo
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Neurodevelopmental Disorder with Dystonia and Chorea Linked to De Novo Variants in the Splicing Regulator SRRM4神经发育障碍伴肌张力障碍和舞蹈症,与剪接调节因子SRRM4的新生变异相关
err2026-04-09
err0
errOAAI
errPhilip Harrer MD, PhD; Volker Kittke PhD; Alice Saparov MSc; Alexej Knaus MD; Shimriet Zeidler MD; Rachel Schot MD; Florian Kraft MD; Matthias Begemann MD; Suzanna Koudijs MD; Ugo Sorrentino MD; Chen Zhao PhD; Ivana Dzinovic PhD; Martin Pavlov MSc; Elisabeth Graf PhD; Antonia M. Stehr MD; Peter M. Krawitz MD; Christian Wilhelm PhD; Saskia Biskup MD; Fahd Alsalloum MD; Steffen Berweck MD; Juliane Winkelmann MD; Konrad Oexle MD; Ingo Kurth MD; G. Christoph Korenke MD; Michael Zech MD
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Systematic analysis of snRNA genes reveals frequent RNU2-2 variants in dominant and recessive developmental and epileptic encephalopathiessnRNA基因的系统分析揭示了显性和隐性发育性和癫痫性脑病中常见的RNU2-2变异
err2026-03-30
err0
errOAAI
errElsa Leitão; Amandine Santini; Benjamin Cogne; Miriam Essid; Maria Athanasiadou; Christy W. LaFlamme; Pierre Marijon; Virginie Bernard; Kevin Jousselin; Nicolas Chatron; Giulia Barcia; Boris Keren; Cyril Mignot; Perrine Charles; Thomas Besnard; Robin Paluch; Jean-Madeleine de Sainte Agathe; Edith P. Almanza Fuerte; Soham Sengupta; Mathieu Milh; Francis Ramond; Talia Allan; Isabelle An; Camila Araujo; Stéphanie Arpin; Christina Austin-Tse; Stéphane Auvin; Sarah Baer; Nadia Bahi-Buisson; Mads Bak; Magalie Barth; Stéphanie Baulac; Nathalie Bednarek-Weirauch; Matthias Begemann; Mark F. Bennett; Uriel Bensabath; Stéphane Bézieau; Rakia Bhouri; Margaux Biehler; Trine Bjørg Hammer; Julie Bogoin; Emilie Bonanno; Simon Boussion; Céline Bris; Adelaide Brosseau-Beauvir; Ange-Line Bruel; Audrey Briand-Suleau; Julien Buratti; Tristan Celse; Pascal Chambon; Nicole Chemaly; Bertrand Chesneau; Estelle Colin; Maxime Colmard; Cindy Colson; Solène Conrad; Thomas Courtin; Isabelle Creveaux; Anne-Charlotte Cullier; Louis T. Dang; Anne de Saint Martin; Caroline de Vanssay de Blavous Legendre; Bénédicte Demeer; Anne-Sophie Denommé-Pichon; Philine Diekhoff; Stephanie DiTroia; Martine Doco-Fenzy; Christèle Dubourg; Charlotte Dubucs; Stéphanie Ducreux; Louis Dufour; Romain Duquet; Benjamin Durand; Salima El Chehadeh; Miriam Elbracht; Laurence Faivre; Marie Faoucher; Anne Faudet; Sylvie Forlani; Mélanie Fradin; Pauline Gaignard; Benjamin Ganne; Aurore Garde; Justine Géraud; Deepak Gill; Alice Goldenberg; David Grabli; Coraline Grisel; Sophie Gueden; Paul Gueguen; Anne-Marie Guerrot; Agnès Guichet; Tobias B. Haack; Nina Härting; Martin Georg Häusler; Solveig Heide; Theresia Herget; Bénédicte Héron; Delphine Héron; Johanna Herwig; Mathilde Heulin; Tess Holling; Clara Houdayer; Bertrand Isidor; Aurélia Jacquette; Louis Januel; Nolwenn Jean-Marçais; Frank J. Kaiser; Sabine Kaya; Chontelle King; Marina Konyukh; Florian Kraft; Jeremias Krause; Rémi Kirstetter; Alma Kuechler; Ingo Kurth; Kerstin Kutsche; Audrey Labalme; Jean-Serene Laloy; Vincent Laugel; Floriane Le Bricquir; Anne-Sophie Lèbre; Marine Lebrun; Eric Leguern; Jonathan Levy; Nico Lieffering; Stanislas Lyonnet; Kevin Lüthy; Sian M. W. Macdonald; Lamisse Mansour-Hendili; Julien Maraval; Iris Marquardt; Carolin Mattausch; Sandra Mercier; Olfa Messaoud; Godelieve Morel; Jérémie Mortreux; Arnold Munnich; Rima Nabbout; Sophie Nambot; Vincent Navarro; Ashana Neale; Laetitia Nguyen; Mathilde Nizon; Frédérique Nowak; Melanie C. O’Leary; Sylvie Odent; Naomi Meave Ojeda; Valérie Olin; Simone Olivieri; Katrin Õunap; Lynn S. Pais; Eleni Panagiotakaki; Olivier Patat; Laurence Perrin-Sabourin; Florence Petit; Christophe Philippe; Amélie Piton; Marc Planes; Céline Poirsier; Antoine Pouzet; Clément Prouteau; Sylvia Quéméner-Redon; Mathilde Renaud; Anne-Claire Richard; Marlène Rio; Clotilde Rivier; Florence Robin-Renaldo; Paul Rollier; Massimiliano Rossi; Agathe Roubertie; Valentin Ruault; Maïlys Rupin-Mas; Pascale Saugier-Veber; Aline Saunier; Russell Saneto; Elisabeth Sarrazin; Catherine Sarret; Elise Schaefer; Caroline Schluth-Bolard; Amy Schneider; Isabell Schumann; Vladimir B. Seplyarskiy; Stephanie Spranger; Thomas Smol; Marc Sturm; Shamil R. Sunyaev; Brian Sperelakis-Beedham; Sarah L. Stenton; Friedrich Stock; Mylène Tharreau; Deniz Torun; Joseph Toulouse; Harshini Thiyagarajah; Stéphanie Valence; Sophie Valleix; Julien Van-Gils; Laurent Villard; Dorothée Ville; Nathalie Villeneuve; Antonio Vitobello; Aurélie Waernessyckle; Jan Wagner; Yvonne Weber; Dagmar Wieczorek; Tom Witkowski; Manya Yadavilli; Tony Yammine; Khaoula Zaafrane-Khachnaoui; Maha S. Zaki; Alban Ziegler; Nuria C. Bramswig; Alban Lermine; Gael Nicolas; Joseph G. Gleeson; Lynette G. Sadleir; Michael S. Hildebrand; Ingrid E. Scheffer; Nicola Whiffin; Anne O’Donnell-Luria; Heather C. Mefford; Pierre Blanc; Julien Thevenon; Camille Charbonnier; Clément Charenton; Christel Depienne; Gaetan Lesca; Caroline Nava
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MDM4 HAPLOINSUFFICIENCY LEADS TO P53-MEDIATED BONE MARROW FAILUREMDM4杂合子不足导致P53介导的骨髓衰竭
errBlood
IF23.1
err2026-03-03
err0
errOAAI
errRicha Sharma; Senthil Velan Bhoopalan; Robert Meyer; Lei Han; Swarna Beesetti; Nana Liu; Priyanka Singh; Lance Palmer; Baranda S. Hansen; Majd Khiami; Lise Larcher; Matthias Begemann; Selim Corbacioglu; Lara Heller; Marcus Jakob; Yan Ju; Sushree S. Sahoo; Nathan Gray; Gabriela Gheorghe; Miriam Elbracht
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Frequent and clinically relevant germline DNA repair gene variants in young and familial myeloproliferative neoplasms年轻型和家族性骨髓增殖性肿瘤中频繁出现且具有临床意义的生殖系DNA修复基因变异
err2026-01-05
err0
errOAAI
errRobert Meyer; Maria Jimena Rodriguez; Madeline Caduc; Kim Kricheldorf; Matthias Begemann; Florian Kraft; Isabel Spier; Daniela Dey; Nergis Güzel; Kerstin Becker; Julian Baumeister; Marcelo A. S. de Toledo; Susanne Isfort; Ulrich Germing; Stefan Aretz; Tim H. Brümmendorf; Ingo Kurth; Miriam Elbracht; Lino L. Teichmann; Steffen Koschmieder
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Author Correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings作者更正: 将下一代表型整合到超早期疾病患者的国家框架中,可改善遗传诊断并产生新的分子发现
err2025-06-24
err0
errOAAI
errAxel Schmidt; Magdalena Danyel; Kathrin Grundmann; Theresa Brunet; Hannah Klinkhammer; Tzung-Chien Hsieh; Hartmut Engels; Sophia Peters; Alexej Knaus; Shahida Moosa; Luisa Averdunk; Felix Boschann; Henrike Lisa Sczakiel; Sarina Schwartzmann; Martin Atta Mensah; Jean Tori Pantel; Manuel Holtgrewe; Annemarie Bösch; Claudia Weiß; Natalie Weinhold; Aude-Annick Suter; Corinna Stoltenburg; Julia Neugebauer; Tillmann Kallinich; Angela M. Kaindl; Susanne Holzhauer; Christoph Bührer; Philip Bufler; Uwe Kornak; Claus-Eric Ott; Markus Schülke; Hoa Huu Phuc Nguyen; Sabine Hoffjan; Corinna Grasemann; Tobias Rothoeft; Folke Brinkmann; Nora Matar; Sugirthan Sivalingam; Claudia Perne; Elisabeth Mangold; Martina Kreiss; Kirsten Cremer; Regina C. Betz; Martin Mücke; Lorenz Grigull; Thomas Klockgether; Isabel Spier; André Heimbach; Tim Bender; Fabian Brand; Christiane Stieber; Alexandra Marzena Morawiec; Pantelis Karakostas; Valentin S. Schäfer; Sarah Bernsen; Patrick Weydt; Sergio Castro-Gomez; Ahmad Aziz; Marcus Grobe-Einsler; Okka Kimmich; Xenia Kobeleva; Demet Önder; Hellen Lesmann; Sheetal Kumar; Pawel Tacik; Meghna Ahuja Bhasin; Pietro Incardona; Min Ae Lee-Kirsch; Reinhard Berner; Catharina Schuetz; Julia Körholz; Tanita Kretschmer; Nataliya Di Donato; Evelin Schröck; André Heinen; Ulrike Reuner; Amalia-Mihaela Hanßke; Frank J. Kaiser; Eva Manka; Martin Munteanu; Alma Kuechler; Kiewert Cordula; Raphael Hirtz; Elena Schlapakow; Christian Schlein; Jasmin Lisfeld; Christian Kubisch; Theresia Herget; Maja Hempel; Christina Weiler-Normann; Kurt Ullrich; Christoph Schramm; Cornelia Rudolph; Franziska Rillig; Maximilian Groffmann; Ania Muntau; Alexandra Tibelius; Eva M. C. Schwaibold; Christian P. Schaaf; Michal Zawada; Lilian Kaufmann; Katrin Hinderhofer; Pamela M. Okun; Urania Kotzaeridou; Georg F. Hoffmann; Daniela Choukair; Markus Bettendorf; Malte Spielmann; Annekatrin Ripke; Martje Pauly; Alexander Münchau; Katja Lohmann; Irina Hüning; Britta Hanker; Tobias Bäumer; Rebecca Herzog; Yorck Hellenbroich; Dominik S. Westphal; Tim Strom; Reka Kovacs; Korbinian M. Riedhammer; Katharina Mayerhanser; Elisabeth Graf; Melanie Brugger; Julia Hoefele; Konrad Oexle; Nazanin Mirza-Schreiber; Riccardo Berutti; Ulrich Schatz; Martin Krenn; Christine Makowski; Heike Weigand; Sebastian Schröder; Meino Rohlfs; Katharina Vill; Fabian Hauck; Ingo Borggraefe; Wolfgang Müller-Felber; Ingo Kurth; Miriam Elbracht; Cordula Knopp; Matthias Begemann; Florian Kraft; Johannes R. Lemke; Julia Hentschel; Konrad Platzer; Vincent Strehlow; Rami Abou Jamra; Martin Kehrer; German Demidov; Stefanie Beck-Wödl; Holm Graessner; Marc Sturm; Lena Zeltner; Ludger J. Schöls; Janine Magg; Andrea Bevot; Christiane Kehrer; Nadja Kaiser; Ernest Turro; Denise Horn; Annette Grüters-Kieslich; Christoph Klein; Stefan Mundlos; Markus Nöthen; Olaf Riess; Thomas Meitinger; Heiko Krude; Peter M. Krawitz; Tobias Haack; Nadja Ehmke; Matias Wagner
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Maternal uniparental disomy of chromosome 7: how chromosome 7-encoded imprinted genes contribute to the Silver-Russell phenotype母系单亲二倍体7号染色体:7号染色体编码的印记基因如何促成Silver-Russell表型
err2025-04-30
err0
errOAAI
errBegemann, Matthias; Lengyel, Anna; Pinti, Eva; Kovacs, Arpad Ferenc; Fekete, Gyorgy; Stratmann, Svea; Krause, Jeremias; Elbracht, Miriam; Kraft, Florian; Eggermann, Thomas
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Benchmarking whole exome sequencing in the German network for personalized medicine评估德国个性化医学网络中的全外显子组测序
err2024-11-01
err1
errOAAI
errMenzel, Michael; Martis-Thiele, Mihaela; Goldschmid, Hannah; Ott, Alexander; Romanovsky, Eva; Siemanowski-Hrach, Janna; Seillier, Lancelot; Bruechle, Nadina Ortiz; Maurer, Angela; Lehmann, Kjong-Van; Begemann, Matthias; Elbracht, Miriam; Meyer, Robert; Dintner, Sebastian; Claus, Rainer; Blanc, Eric; Moebs, Markus; Joosten, Maria; Basitta, Patrick; Hoelscher, Florian; Tischler, Verena; Gross, Thomas; Kutz, Oliver; Prause, Rebecca; William, Doreen; Horny, Kai; Goering, Wolfgang; Borkhardt, Arndt; Blank, Cornelia; Junk, Stefanie V.; Yasin, Layal; Moskalev, Evgeny A.; Ferrazzi, Fulvia; Toegel, Lars; Wolter, Steffen; Adam, Eugen; Matysiak, Uta; Rosenthal, Tessa; Doenitz, Juergen; Lehmann, Ulrich; Schmidt, Gunnar; Hofmann, Winfried; Hirsch, Steffen; Dikow, Nicola; Goebel, Kirsten; Banan, Rouzbeh; Hamelmann, Stefan; Fink, Annette; Ball, Markus; Neumann, Olaf; Rehker, Jan; Kloth, Michael; Murtagh, Justin; Hartmann, Nils; Jurmeister, Phillip; Mock, Andreas; Kumbrink, Joerg; Jung, Andreas; Mayr, Eva-Maria; Jacob, Anne; Trautmann, Marcel; Kirmse, Santina; Falkenberg, Kim; Ruckert, Christian; Hirsch, Daniela; Immel, Alexander; Dietmaier, Wolfgang; Haack, Tobias; Marienfeld, Ralf; Fuerstberger, Axel; Niewoehner, Jakob; Gerstenmaier, Uwe; Eberhardt, Timo; Greif, Philipp A.; Appenzeller, Silke; Maurus, Katja; Doll, Julia; Jelting, Yvonne; Jonigk, Danny; Maerkl, Bruno; Beule, Dieter; Horst, David; Wulf, Anna-Lena; Aust, Daniela; Werner, Martin; Reuter-Jessen, Kirsten; Stroebel, Philipp; Auber, Bernd; Merkelbach-Bruse, Sabine; Siebolts, Udo; Roth, Wilfried; Lassmann, Silke; Klauschen, Frederick; Gaisa, Nadine T.; Weichert, Wilko; Evert, Matthias; Armeanu-Ebinger, Sorin; Ossowski, Stephan; Schroeder, Christopher; Schaaf, Christian P.; Malek, Nisar; Schirmacher, Peter; Kazdal, Daniel; Pfarr, Nicole; Budczies, Jan; Stenzinger, Albrecht
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Complex structural variation and nonsense variant in trans cause VPS50-related disorder
err2024-06-14
err0
PREAI
errHecher, Laura; Gorski-Alberts, Esther; Begemann, Matthias; Herwig, Johanna; Lausberg, Eva; Hillebrand, Georg; Volk, Alexander E.; Kurth, Ingo; Kraft, Florian; Kutsche, Kerstin
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De novo variants in RNF213 are associated with a clinical spectrum ranging from Leigh syndrome to early-onset strokeRNF213的De novo变异与从Leigh综合征到早发性中风的临床范围相关
err2024-02-01
err5
PREAI
errBrunet, Theresa; Zott, Benedikt; Lieftuchter, Victoria; Lenz, Dominic; Schmidt, Axel; Peters, Philipp; Kopajtich, Robert; Zaddach, Malin; Zimmermann, Hanna; Huning, Irina; Ballhausen, Diana; Staufner, Christian; Bianzano, Alyssa; Hughes, Joanne; Taylor, Robert W.; McFarland, Robert; Devlin, Anita; MihaljeviC, Mihaela; Barisic, Nina; Rohlfs, Meino; Wilfling, Sibylle; Sondheimer, Neal; Hewson, Stacy; Marinakis, Nikolaos M.; Kosma, Konstantina; Traeger-Synodinos, Joanne; Elbracht, Miriam; Begemann, Matthias; Trepels-Kottek, Sonja; Hasan, Dimah; Scala, Marcello; Capra, Valeria; Zara, Federico; van der Ven, Amelie T.; Driemeyer, Joenna; Apitz, Christian; Kramer, Johannes; Strong, Alanna; Hakonarson, Hakon; Watson, Deborah; Mayr, Johannes A.; Prokisch, Holger; Meitinger, Thomas; Borggraefe, Ingo; Spiegler, Juliane; Baric, Ivo; Paolini, Marco; Gerstl, Lucia; Wagner, Matias
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Genetic landscape of congenital insensitivity to pain and hereditary sensory and autonomic neuropathies
errBRAIN
IF11.7
err2023-09-28
err6
errOAAI
errLischka, Annette; Eggermann, Katja; Record, Christopher J.; Dohrn, Maike F.; Lassuthova, Petra; Kraft, Florian; Begemann, Matthias; Dey, Daniela; Eggermann, Thomas; Beijer, Danique; Soukalova, Jana; Laura, Matilde; Rossor, Alexander M.; Mazanec, Radim; Van Lent, Jonas; Tomaselli, Pedro J.; Ungelenk, Martin; Debus, Karlien Y.; Feely, Shawna M. E.; Glaeser, Dieter; Jagadeesh, Sujatha; Martin, Madelena; Govindaraj, Geeta M.; Singhi, Pratibha; Baineni, Revanth; Biswal, Niranjan; Ibarra-Ramirez, Marisol; Bonduelle, Maryse; Gess, Burkhard; Romero Sanchez, Juan; Suthar, Renu; Udani, Vrajesh; Nalini, Atchayaram; Unnikrishnan, Gopikrishnan; Marques Junior, Wilson; Mercier, Sandra; Procaccio, Vincent; Bris, Celine; Suresh, Beena; Reddy, Vaishnavi; Skorupinska, Mariola; Bonello-Palot, Nathalie; Mochel, Fanny; Dahl, Georg; Sasidharan, Karthika; Devassikutty, Fiji M.; Nampoothiri, Sheela; Rodovalho Doriqui, Maria J.; Mueller-Felber, Wolfgang; Vill, Katharina; Haack, Tobias B.; Dufke, Andreas; Abele, Michael; Stucka, Rolf; Siddiqi, Saima; Ullah, Noor; Spranger, Stephanie; Chiabrando, Deborah; Bolgul, Behiye S.; Parman, Yesim; Seeman, Pavel; Lampert, Angelika; Schulz, Joerg B.; Wood, John N.; Cox, James J.; Auer-Grumbach, Michaela; Timmerman, Vincent; de Winter, Jonathan; Themistocleous, Andreas C.; Shy, Michael; Bennett, David L.; Baets, Jonathan; Huebner, Christian A.; Leipold, Enrico; Zuchner, Stephan; Elbracht, Miriam; Cakar, Arman; Senderek, Jan; Hornemann, Thorsten; Woods, C. Geoffrey; Reilly, Mary M.; Kurth, Ingo
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Imprinting disorders
err2023-06-29
err22
PREAI
errEggermann, Thomas; Monk, David; de Nanclares, Guiomar Perez; Kagami, Masayo; Giabicani, Eloise; Riccio, Andrea; Tumer, Zeynep; Kalish, Jennifer M.; Tauber, Maithe; Duis, Jessica; Weksberg, Rosanna; Maher, Eamonn R.; Begemann, Matthias; Elbracht, Miriam
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DDX41 germline variants causing donor cell leukemia indicate a need for further genetic workup in the context of hematopoietic stem cell transplantation
err2023-05-10
err7
errOAAI
errRolles, Benjamin; Meyer, Robert; Begemann, Matthias; Elbracht, Miriam; Jost, Edgar; Stelljes, Matthias; Kurth, Ingo; Bruemmendorf, Tim H.; Silling, Gerda
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Identification of Adult Patients With Classical Dyskeratosis Congenita or Cryptic Telomere Biology Disorder by Telomere Length Screening Using Age-modified Criteria
err2023-05-01
err6
errOAAI
errTometten, Mareike; Kirschner, Martin; Meyer, Robert; Begemann, Matthias; Halfmeyer, Insa; Vieri, Margherita; Kricheldorf, Kim; Maurer, Angela; Platzbecker, Uwe; Radsak, Markus; Schafhausen, Philippe; Corbacioglu, Selim; Hoechsmann, Britta; Wilk, C. Matthias; Hinze, Claas; Chromik, Joerg; Heuser, Michael; Kreuter, Michael; Koschmieder, Steffen; Panse, Jens; Isfort, Susanne; Kurth, Ingo; Bruemmendorf, Tim H.; Beier, Fabian
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Molecular characterisation of 36 multilocus imprinting disturbance (MLID) patients: a comprehensive approach
err2023-03-01
err5
errOAAI
errBilo, Larissa; Ochoa, Eguzkine; Lee, Sunwoo; Dey, Daniela; Kurth, Ingo; Kraft, Florian; Rodger, Fay; Docquier, France; Toribio, Ana; Bottolo, Leonardo; Binder, Gerhard; Fekete, Gyoergy; Elbracht, Miriam; Maher, Eamonn R.; Begemann, Matthias; Eggermann, Thomas
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