Constitutional mismatch repair-deficiency syndrome

le Wimmer, Katharina, Kratz, Christian P.
Foilsithe 2010

The clinical utility of testicular cancer risk loci

le Kratz, Christian P, Bratslavsky, Gennady, Shi, Jianxin
Foilsithe 2011

An unexpected new role of mutant Ras: perturbation of human embryonic development

le Kratz, Christian P., Niemeyer, Charlotte M., Zenker, Martin
Foilsithe 2007

Familial Testicular Germ Cell Tumors

le Kratz, Christian P., Mai, Phuong L., Greene, Mark H.
Foilsithe 2010

Cancer in Noonan, Costello, Cardiofaciocutaneous and LEOPARD Syndromes

le Kratz, Christian P., Rapisuwon, Suthee, Reed, Helen, Hasle, Henrik, Rosenberg, Philip S.
Foilsithe 2011

Promoter methylation of candidate genes associated with familial testicular cancer

le Mirabello, Lisa, Kratz, Christian P, Savage, Sharon A, Greene, Mark H
Foilsithe 2012

Clinical utility gene card for: Familial platelet disorder with associated myeloid malignancies

le Ripperger, Tim, Tawana, Kiran, Kratz, Christian, Schlegelberger, Brigitte, Fitzgibbon, Jude, Steinemann, Doris
Foilsithe in Eur J Hum Genet (2016)

Cancer surveillance for individuals with Li-Fraumeni syndrome

le Kratz, Christian P., Villani, Anita, Nichols, Kim E., Schiffman, Joshua, Malkin, David
Foilsithe in Eur J Hum Genet (2020)

Juvenile Myelomonocytic Leukemia: A Report from the 2(nd) International JMML Symposium

le Chan, Rebecca J., Cooper, Todd, Kratz, Christian P., Weiss, Brian, Loh, Mignon L.
Foilsithe 2008

Genetic and epigenetic analysis of monozygotic twins discordant for testicular cancer

le Kratz, Christian P, Edelman, Daniel C, Wang, Yonghong, Meltzer, Paul S, Greene, Mark H
Foilsithe 2014

PMS2 inactivation by a complex rearrangement involving an HERV retroelement and the inverted 100-kb duplicon on 7p22.1

le Vogt, Julia, Wernstedt, Annekatrin, Ripperger, Tim, Pabst, Brigitte, Zschocke, Johannes, Kratz, Christian, Wimmer, Katharina
Foilsithe in Eur J Hum Genet (2016)

Close ties: an exploratory Colored Eco-Genetic Relationship Map (CEGRM) study of social connections of men in Familial Testicular Cancer (FTC) families

le Peters, June A, Kenen, Regina, Hoskins, Lindsey M, Glenn, Gladys M, Kratz, Christian, Greene, Mark H
Foilsithe 2012

Long-term outcome of hemizygous and heterozygous carriers of a germline GATA1(G208R) mutation

le Dührsen, Ulrich, Kratz, Christian P., Flotho, Christian, Lauenstein, Thomas, Bommer, Martin, König, Erika, Brittinger, Günter, Heimpel, Hermann
Foilsithe 2010

Human PMS2 deficiency is associated with impaired immunoglobulin class switch recombination

le Péron, Sophie, Metin, Ayse, Gardès, Pauline, Alyanakian, Marie-Alexandra, Sheridan, Eamonn, Kratz, Christian Peter, Fischer, Alain, Durandy, Anne
Foilsithe 2008

Biochemical and Functional Characterization of Germ Line KRAS Mutations

le Schubbert, Suzanne, Bollag, Gideon, Lyubynska, Natalya, Nguyen, Hoa, Kratz, Christian P., Zenker, Martin, Niemeyer, Charlotte M., Molven, Anders, Shannon, Kevin
Foilsithe 2007

Germline KRAS Mutations Cause Aberrant Biochemical and Physical Properties Leading to Developmental Disorders

le Gremer, Lothar, Merbitz-Zahradnik, Torsten, Dvorsky, Radovan, Cirstea, Ion C., Kratz, Christian Peter, Zenker, Martin, Wittinghofer, Alfred, Ahmadian, Mohammad Reza
Foilsithe 2010

Erythrocyte Adenosine Deaminase: Diagnostic Value for Diamond-Blackfan Anaemia

le Fargo, John H., Kratz, Christian P., Giri, Neelam, Savage, Sharon A., Wong, Carolyn, Backer, Karen, Alter, Blanche P., Glader, Bertil
Foilsithe 2012

Need for a precise molecular diagnosis in Beckwith-Wiedemann and Silver-Russell syndrome: what has to be considered and why it is important

le Eggermann, Thomas, Brück, Johanna, Knopp, Cordula, Fekete, György, Kratz, Christian, Tasic, Velibor, Kurth, Ingo, Elbracht, Miriam, Eggermann, Katja, Begemann, Matthias
Foilsithe in J Mol Med (Berl) (2020)

Cancer prevention by aspirin in children with Constitutional Mismatch Repair Deficiency (CMMRD)

le Leenders, Erika K. S. M., Westdorp, Harm, Brüggemann, Roger J., Loeffen, Jan, Kratz, Christian, Burn, John, Hoogerbrugge, Nicoline, Jongmans, Marjolijn C. J.
Foilsithe in Eur J Hum Genet (2018)

T-cell Acute Lymphoblastic Leukemia in Association with Börjeson-Forssman-Lehmann Syndrome Due to a Mutation in PHF6

le Chao, Mwe Mwe, Todd, Matthew A., Kontny, Udo, Neas, Katherine, Sullivan, Michael J., Hunter, Alasdair G., Picketts, David J., Kratz, Christian P.
Foilsithe 2010