Результаты поиска - Kratz, Christian
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Constitutional mismatch repair-deficiency syndrome по Wimmer, Katharina, Kratz, Christian P.
Опубликовано 2010Текст -
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The clinical utility of testicular cancer risk loci по Kratz, Christian P, Bratslavsky, Gennady, Shi, Jianxin
Опубликовано 2011Текст -
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Familial Testicular Germ Cell Tumors по Kratz, Christian P., Mai, Phuong L., Greene, Mark H.
Опубликовано 2010Текст -
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Choose and stay on one out of two paths: distinction between clinical versus research genetic testing to identify cancer predisposition syndromes among patients with cancer по Ripperger, Tim, Evans, D Gareth, Malkin, David, Kratz, Christian P.
Опубликовано 2021Текст -
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Correction to: Choose and stay on one out of two paths: distinction between clinical versus research genetic testing to identify cancer predisposition syndromes among patients with... по Ripperger, Tim, Evans, D. Gareth, Malkin, David, Kratz, Christian P.
Опубликовано 2021Текст -
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Proportion of children with cancer that have an indication for genetic counseling and testing based on the cancer type irrespective of other features по Nguyen, Thi Minh Kha, Behnert, Astrid, Pietsch, Torsten, Vokuhl, Christian, Kratz, Christian Peter
Опубликовано 2021Текст -
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PMS2 inactivation by a complex rearrangement involving an HERV retroelement and the inverted 100-kb duplicon on 7p22.1 по Vogt, Julia, Wernstedt, Annekatrin, Ripperger, Tim, Pabst, Brigitte, Zschocke, Johannes, Kratz, Christian, Wimmer, Katharina
Опубликовано 2016Текст -
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Close ties: an exploratory Colored Eco-Genetic Relationship Map (CEGRM) study of social connections of men in Familial Testicular Cancer (FTC) families по Peters, June A, Kenen, Regina, Hoskins, Lindsey M, Glenn, Gladys M, Kratz, Christian, Greene, Mark H
Опубликовано 2012Текст -
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Long-term outcome of hemizygous and heterozygous carriers of a germline GATA1(G208R) mutation по Dührsen, Ulrich, Kratz, Christian P., Flotho, Christian, Lauenstein, Thomas, Bommer, Martin, König, Erika, Brittinger, Günter, Heimpel, Hermann
Опубликовано 2010Текст -
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Human PMS2 deficiency is associated with impaired immunoglobulin class switch recombination по Péron, Sophie, Metin, Ayse, Gardès, Pauline, Alyanakian, Marie-Alexandra, Sheridan, Eamonn, Kratz, Christian Peter, Fischer, Alain, Durandy, Anne
Опубликовано 2008Текст