Ohcanbohtosat - Christian P. Kratz
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Constitutional mismatch repair-deficiency syndrome Dahkki Katharina Wimmer, Christian P. Kratz
Almmustuhtton 2010Carta -
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The clinical utility of testicular cancer risk loci Dahkki Christian P. Kratz, Gennady Bratslavsky, Jianxin Shi
Almmustuhtton 2011Editorial -
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Cancer in Noonan, Costello, cardiofaciocutaneous and LEOPARD syndromes Dahkki Christian P. Kratz, Suthee Rapisuwon, Helen E. Reed, Henrik Hasle, Philip S. Rosenberg
Almmustuhtton 2011Artigo -
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Human PMS2 deficiency is associated with impaired immunoglobulin class switch recombination Dahkki Sophie Péron, Ayşe Metìn, Pauline Gardës, Marie‐Alexandra Alyanakian, Eamonn Sheridan, Christian P. Kratz, Alain Fischer, Anne Durandy
Almmustuhtton 2008Artigo -
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ERN GENTURIS guidelines on constitutional mismatch repair deficiency diagnosis, genetic counselling, surveillance, quality of life, and clinical management Dahkki Chrystelle Colas, Léa Guerrini‐Rousseau, Manon Suerink, Richard Gallon, Christian P. Kratz, Éloïse Ayuso, Laurence Brugières, Katharina Wimmer
Almmustuhtton 2024Revisão -
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Germline KRAS mutations cause aberrant biochemical and physical properties leading to developmental disorders Dahkki Lothar Gremer, Torsten Merbitz-Zahradnik, Radovan Dvorský, Ion Cristian Cirstea, Christian P. Kratz, Martin Zenker, Alfred Wittinghofer, Mohammad Reza Ahmadian
Almmustuhtton 2010Artigo -
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Genome-wide single-nucleotide polymorphism analysis in juvenile myelomonocytic leukemia identifies uniparental disomy surrounding the NF1 locus in cases associated with neurofibrom... Dahkki Christian Flotho, Doris Steinemann, Charles G. Mullighan, Geoffrey Neale, Karin Mayer, Christian P. Kratz, Brigitte Schlegelberger, James R. Downing, Charlotte M. Niemeyer
Almmustuhtton 2007Artigo -
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Cancer in Children With Fanconi Anemia and Ataxia-Telangiectasia—A Nationwide Register-Based Cohort Study in Germany Dahkki Christina M. Dutzmann, Claudia Spix, I Popp, Melanie Kaiser, Friederike Erdmann, Miriam Erlacher, Thilo Dörk, Detlev Schindler, Reinhard Kalb, Christian P. Kratz
Almmustuhtton 2021Artigo -
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Health‐related quality of life and fear of progression in individuals with <scp>Li‐Fraumeni</scp> syndrome Dahkki Senta Kiermeier, Sarah Schott, Juliane Nees, Christina Dutzmann, Farina Josepha Strüwe, Christian P. Kratz, Christina Sauer, Anna Fleischer, Myriam Keymling, Imad Maatouk
Almmustuhtton 2024Artigo -
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Variants in or near KITLG, BAK1, DMRT1, and TERT-CLPTM1L predispose to familial testicular germ cell tumour Dahkki Christian P. Kratz, Summer S. Han, Philip S. Rosenberg, Sonja I. Berndt, Laura Burdett, Matthew Yeager, Larissa A. Korde, P. L., Ruth M. Pfeiffer, Mark H. Greene
Almmustuhtton 2011Artigo -
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Myopathy caused by HRAS germline mutations: implications for disturbed myogenic differentiation in the presence of constitutive HRas activation Dahkki I. van der Bürgt, William J. Kupsky, Stephani Stassou, Ali M. Nadroo, Cândida Barroso, Anja Diem, Christian P. Kratz, Radovan Dvorský, Mohammad Reza Ahmadian, Martin Zenker
Almmustuhtton 2007Carta -
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Genotype-phenotype correlation in cases of juvenile myelomonocytic leukemia with clonal RAS mutations Dahkki Christian Flotho, Christian P. Kratz, Eva Bergsträßer, Henrik Hasle, Jan Starý, Monika Trebo, Marry M. van den Heuvel‐Eibrink, Dorota Wójcik, Marco Zecca, Franco Locatelli, Charlotte M. Niemeyer
Almmustuhtton 2008Carta -
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A novel germline POLE mutation causes an early onset cancer prone syndrome mimicking constitutional mismatch repair deficiency Dahkki Katharina Wimmer, Andreas Beilken, R. Nustede, Tim Ripperger, Britta Lamottke, Benno Ure, Diana Steinmann, Tanja Reineke‐Plaaß, Ulrich Lehmann, Johannes Zschocke, Laura Valle, Christine Fauth, Christian P. Kratz
Almmustuhtton 2016Artigo -
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Next Generation Sequencing and Pediatric Brain Tumors: Detection of Cancer Predisposition Syndromes in Patients and Their Families Dahkki Kerstin Grund, Dominik Sturm, Christian Sutter, Felix Sahm, Katrin Hinderhofer, Christian P. Kratz, Daniel Schrimpf, Andreas von Deimling, Kristian W. Pajtler, David Jones, Stefan M. Pfister, Nicola Dikow
Almmustuhtton 2017Artigo
Ohcanreaiddut:
Laktáseaddji fáttát
Biology
Medicine
Genetics
Gene
Internal medicine
Cancer
Mutation
Oncology
Germline mutation
Germline
Cancer research
KRAS
Pathology
Colorectal cancer
Genotype
Phenotype
Noonan syndrome
Pediatrics
Allele
Costello syndrome
DNA mismatch repair
Cohort
Genetic testing
Stem cell
Haematopoiesis
Immunology
Intensive care medicine
PMS2
PTPN11
Single-nucleotide polymorphism