Identification of Adult Patients With Classical Dyskeratosis Congenita or Cryptic Telomere Biology Disorder by Telomere Length Screening Using Age‐modified Criteria
Tometten, Mareike, Kirschner, Martin, Meyer, Robert, Begemann, Matthias, Halfmeyer, Insa, Vieri, Margherita, Kricheldorf, Kim, Maurer, Angela, Platzbecker, Uwe, Radsak, Markus, Schafhausen, Philippe, Corbacioglu, Selim, Höchsmann, Britta, Matthias Wilk, C., Hinze, Claas, Chromik, Jörg, Heuser, Michael, Kreuter, Michael, Koschmieder, Steffen, Panse, Jens, Isfort, Susanne, Kurth, Ingo, Brümmendorf, Tim H., Beier, Fabian
Published in HemaSphere (01.05.2023)
Published in HemaSphere (01.05.2023)
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Comparison of flow‐FISH and MM–qPCR telomere length assessment techniques for the screening of telomeropathies
Ferreira, Monica S. Ventura, Kirschner, Martin, Halfmeyer, Insa, Estrada, Natalia, Xicoy, Blanca, Isfort, Susanne, Vieri, Margherita, Zamora, Lurdes, Abels, Anne, Bouillon, Anne‐Sophie, Begemann, Matthias, Schemionek, Mirle, Maurer, Angela, Koschmieder, Steffen, Wilop, Stefan, Panse, Jens, Brümmendorf, Tim H., Beier, Fabian
Published in Annals of the New York Academy of Sciences (01.04.2020)
Published in Annals of the New York Academy of Sciences (01.04.2020)
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Approach to Cohort-Wide Re-Analysis of Exome Data in 1000 Individuals with Neurodevelopmental Disorders
Halfmeyer, Insa, Bartolomaeus, Tobias, Popp, Bernt, Radtke, Maximilian, Helms, Tobias, Hentschel, Julia, Popp, Denny, Jamra, Rami Abou
Published in Genes (22.12.2022)
Published in Genes (22.12.2022)
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Clinical Presentation of Patients with Adult Late-Onset Telomere Biology Disorders - Results from the Aachen Telomeropathy Registry
Beier, Fabian, Tometten, Mareike, Kirschner, Martin, Halfmeyer, Insa, Vieri, Margherita, Kricheldorf, Kim, Maurer, Angela, Roeth, Alexander, Platzbecker, Uwe, Radsak, Markus P., Schafhausen, Philippe, Corbacioglu, Selim, Hoechsmann, Britta, Wilk, C. Matthias, Hinze, Claas, Chromik, Jörg, Egle, Alexander, Heuser, Michael, Kreuter, Michael, Kurth, Ingo, Koschmieder, Steffen, Panse, Jens, Meyer, Robert, Isfort, Susanne, Brummendorf, Tim H
Published in Blood (23.11.2021)
Published in Blood (23.11.2021)
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Recurrent somatic mutations are rare in patients with cryptic dyskeratosis congenita
Kirschner, Martin, Maurer, Angela, Wlodarski, Marcin W., Ventura Ferreira, Monica S., Bouillon, Anne-Sophie, Halfmeyer, Insa, Blau, Wolfgang, Kreuter, Michael, Rosewich, Martin, Corbacioglu, Selim, Beck, Joachim, Schwarz, Michaela, Bittenbring, Jörg, Radsak, Markus P., Wilk, Christian Matthias, Koschmieder, Steffen, Begemann, Matthias, Kurth, Ingo, Schemionek, Mirle, Brümmendorf, Tim H., Beier, Fabian
Published in Leukemia (01.08.2018)
Published in Leukemia (01.08.2018)
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