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Hearle, N, Schumacher, V, Menko, F H, Olschwang, S, Boardman, L A, Gille, J J P, Keller, J J, Westerman, A M, Scott, R J, Lim, W, Trimbath, J D, Giardiello, F M, Gruber, S B, Offerhaus, G J A, Rooij, F W M D E, Wilson, J H P, Hansmann, A, Möslein, G, Royer-Pokora, B, Vogel, T, Phillips, R K S, Spigelman, A D, Houlston, R S
Published in Journal of medical genetics (01.08.2006)
Published in Journal of medical genetics (01.08.2006)
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Correlation of germ-line mutations and two-hit inactivation of the WT1 gene with Wilms tumors of stromal–predominant histology
Schumacher, V, Schneider, S, Figge, A, Wildhardt, G, Harms, D, Schmidt, D, Weirich, A, Ludwig, R, Royer-Pokora, B
Published in Proceedings of the National Academy of Sciences - PNAS (15.04.1997)
Published in Proceedings of the National Academy of Sciences - PNAS (15.04.1997)
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Recessive missense mutations in LAMB2 expand the clinical spectrum of LAMB2-associated disorders
Hasselbacher, K., Wiggins, R.C., Matejas, V., Hinkes, B.G., Mucha, B., Hoskins, B.E., Ozaltin, F., Nürnberg, G., Becker, C., Hangan, D., Pohl, M., Kuwertz-Bröking, E., Griebel, M., Schumacher, V., Royer-Pokora, B., Bakkaloglu, A., Nürnberg, P., Zenker, M., Hildebrandt, F.
Published in Kidney international (01.09.2006)
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Comprehensive array CGH of normal karyotype myelodysplastic syndromes reveals hidden recurrent and individual genomic copy number alterations with prognostic relevance
Thiel, A, Beier, M, Ingenhag, D, Servan, K, Hein, M, Moeller, V, Betz, B, Hildebrandt, B, Evers, C, Germing, U, Royer-Pokora, B
Published in Leukemia (01.03.2011)
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STK11 genotyping and cancer risk in Peutz-Jeghers syndrome
Schumacher, V, Vogel, T, Leube, B, Driemel, C, Goecke, T, Möslein, G, Royer-Pokora, B
Published in Journal of medical genetics (01.05.2005)
Published in Journal of medical genetics (01.05.2005)
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SDHD mutation analysis in seven German patients with sporadic carotid body paraganglioma: one novel mutation, no Dutch founder mutation and further evidence that G12S is a polymorphism
Leube, B, Huber, R, Goecke, TO, Sandmann, W, Royer-Pokora, B
Published in Clinical genetics (01.01.2004)
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Survival in nephroblastoma treated according to the trial and study SIOP-9/GPOH with respect to relapse and morbidity
Weirich, A., Ludwig, R., Graf, N., Abel, U., Leuschner, I., Vujanic, G. M., Mehls, O., Boos, J., Beck, J., Royer-Pokora, B., Voûte, P. A.
Published in Annals of oncology (01.05.2004)
Published in Annals of oncology (01.05.2004)
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Ten novel mutations found in aniridia
Wolf, Matthias T. F., Lorenz, B, Winterpacht, A, Drechsler, M, Schumacher, V, Royer-Pokora, B, Blankenagel, A, Zabel, B, Wildhardt, G
Published in Human mutation (1998)
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160 ANALYSIS OF POSSIBLE BIOMARKERS TO PREDICT RESPONSE IN PATIENTS WITH MYELODYSPLASTIC SYNDROMES OR ACUTE MYELOID LEUKEMIA TREATED WITH 5-AZACITIDINE
Kuendgen, A, Müller-Thomas, C, Lauseker, M, Urbaniak, P, Haferlach, T, Alpermann, T, Meggendorfer, M, Schnittger, S, Brings, C, Wulfert, M, Hildebrandt, B, Betz, B, Royer-Pokora, B, Haas, R, Gattermann, N, Germing, U, Götze, K
Published in Leukemia research (01.04.2015)
Published in Leukemia research (01.04.2015)
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Colorectal Carcinoma with Suspected Lynch Syndrome: A Multidisciplinary Algorithm
Schneider, R, Schneider, C, Büttner, R, Reinacher-Schick, A, Tannapfel, A, Fürst, A, Rüschoff, J, Jakobeit, C, Royer-Pokora, B, Möslein, G
Published in Zentralblatt fur Chirurgie (01.12.2015)
Published in Zentralblatt fur Chirurgie (01.12.2015)
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A novel transcript of the LMO2 gene, LMO2-c, is regulated by GATA-1 and PU.1 and encodes an antagonist of LMO2
WANG, Q, ZHANG, M, WANG, X, YUAN, W, CHEN, D, ROYER-POKORA, B, ZHU, T
Published in Leukemia (01.05.2007)
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Shared Copy Number Variation in Simultaneous Nephroblastoma and Neuroblastoma due to Fanconi Anemia
Serra, A., Eirich, K., Winkler, A.K., Mrasek, K., Göhring, G., Barbi, G., Cario, H., Schlegelberger, B., Royer-Pokora, B., Liehr, T., Leriche, C., Henne-Bruns, D., Barth, T.F., Schindler, D.
Published in Molecular syndromology (01.09.2012)
Published in Molecular syndromology (01.09.2012)
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The size of the CAG repeat in exon 1 of the androgen receptor gene shows no significant relationship to impaired spermatogenesis in an infertile Caucasoid sample of German origin
Dadze, S., Wieland, C., Jakubiczka, S., Funke, K., Schröder, E., Royer-Pokora, B., Willers, R., Wieacker, P.F.
Published in Molecular human reproduction (01.03.2000)
Published in Molecular human reproduction (01.03.2000)
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Gene expression profiling of Philadelphia chromosome (Ph)-negative CD34+ hematopoietic stem and progenitor cells of patients with Ph-positive CML in major molecular remission during therapy with imatinib
NEUMANN, F, TEUTSCH, N, ROYER-POKORA, B, EILS, R, GATTERMANN, N, HAAS, R, KRONENWETT, R, KLISZEWSKI, S, BORK, S, STEIDL, U, BRORS, B, SCHIMKUS, N, ROES, N, GERMING, U, HILDEBRANDT, B
Published in Leukemia (01.03.2005)
Published in Leukemia (01.03.2005)
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Simultaneous occurrence of a t(9;22) (Ph) with a t(2;11) in a patient with CML and emergence of a new clone with the t(2;11) alone after imatinib mesylate treatment
Royer-Pokora, B, Hildebrandt, B, Redmann, A, Herold, C, Kronenwett, R, Haas, R, Drechsler, M, Wieland, C
Published in Leukemia (01.04.2003)
Published in Leukemia (01.04.2003)
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Evidence for susceptibility genes to familial Wilms tumour in addition to WT1, FWT1 and FWT2
RAPLEY, E. A, BARFOOT, R, SKEEN, J, DE TOURRELL, S, WEIRICH, A, PRITCHARD-JONES, K, STRATTON, M. R, RAHMAN, N, BONAÏTI-PELLIE, C, CHOMPRET, A, FOULKES, W, PERUSINGHE, N, REEVE, A, ROYER-POKORA, B, SCHUMACHER, V, SHELLING, A
Published in British journal of cancer (01.07.2000)
Published in British journal of cancer (01.07.2000)
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P-67 Hyperdiploidy in MDS and AML is associated with poor prognosis
Balleisen, S., Knipp, S., Kuendgen, A., Hildebrandt, B., Gattermann, N., Haas, R., Royer-Pokora, B., Genning, U.
Published in Leukemia research (2005)
Published in Leukemia research (2005)
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