Cancer spectrum and frequency among children with Noonan, Costello, and cardio-facio-cutaneous syndromes
Kratz, C P, Franke, L, Peters, H, Kohlschmidt, N, Kazmierczak, B, Finckh, U, Bier, A, Eichhorn, B, Blank, C, Kraus, C, Kohlhase, J, Pauli, S, Wildhardt, G, Kutsche, K, Auber, B, Christmann, A, Bachmann, N, Mitter, D, Cremer, F W, Mayer, K, Daumer-Haas, C, Nevinny-Stickel-Hinzpeter, C, Oeffner, F, Schlüter, G, Gencik, M, Überlacker, B, Lissewski, C, Schanze, I, Greene, M H, Spix, C, Zenker, M
Published in British journal of cancer (14.04.2015)
Published in British journal of cancer (14.04.2015)
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Rothmund–Thomson syndrome type 1 caused by biallelic ANAPC1 gene mutations
Zirn, B., Bernbeck, U., Alt, K., Oeffner, F., Gerhardinger, A., Has, C.
Published in Skin health and disease (01.03.2021)
Published in Skin health and disease (01.03.2021)
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Systematic screening for mutations in the human necdin gene (NDN): identification of two naturally occurring polymorphisms and association analysis in body weight regulation
OEFFNER, F, KORN, T, ROTH, H, ZIEGLER, A, HINNEY, A, GOLDSCHMIDT, H, SIEGFRIED, W, HEBEBRAND, J, GRZESCHIK, K-H
Published in International Journal of Obesity (01.06.2001)
Published in International Journal of Obesity (01.06.2001)
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Significant association between a silent polymorphism in the neuromedin B gene and body weight in German children and adolescents
OEFFNER, F, BORNHOLDT, D, GRZESCHIK, K. H, ZIEGLER, A, HINNEY, A, GÖRG, T, GERBER, G, GOLDSCHMIDT, H. P, SIEGFRIED, W, WRIGHT, A, HEBEBRAND, J
Published in Acta diabetologica (2000)
Published in Acta diabetologica (2000)
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CHARACTERIZATION OF DUVELISIB IN PATIENTS WITH REFRACTORY MARGINAL ZONE LYMPHOMA: DATA FROM THE PHASE 2 DYNAMO TRIAL
Jacobsen, E., Ďuraš, J., Ardeshna, K., Cherry, M., Offner, F., Mayer, J., Bijou, F., Tani, M., Musuraca, G., Merli, M., Marasca, R., Weaver, D.T., Lustgarten, S., Youssoufian, H., Zinzani, P.
Published in Hematological oncology (01.06.2019)
Published in Hematological oncology (01.06.2019)
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Novel interaction partners of Bardet-Biedl syndrome proteins
Oeffner, F, Moch, C, Neundorf, A, Hofmann, J, Koch, M, Grzeschik, K H
Published in Cell motility and the cytoskeleton (01.02.2008)
Published in Cell motility and the cytoskeleton (01.02.2008)
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Journal Article
Multiple familial trichoepithelioma caused by mutations in the cylindromatosis tumor suppressor gene
SALHI, Aicha, BORNHOLDT, Dorothea, OEFFNER, Frank, MALIK, Sajid, HEID, Ernest, HAPPLE, Rudolf, GRZESCHIK, Karl-Heinz
Published in Cancer research (Chicago, Ill.) (01.08.2004)
Published in Cancer research (Chicago, Ill.) (01.08.2004)
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Journal Article
Common infectious agents in multiple sclerosis: a case—control study in children
Krone, Bernd, Pohl, Daniela, Rostasy, Kevin, Kahler, Elke, Brunner, Edgar, Oeffner, Frank, Grange, John M., Gärtner, Jutta, Hanefeld, Folker
Published in Multiple sclerosis (01.01.2008)
Published in Multiple sclerosis (01.01.2008)
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Journal Article
Independent confirmation of a major locus for obesity on chromosome 10
HINNEY, A, ZIEGLER, A, REMSCHMIDT, H, HEBEBRAND, J, OEFFNER, F, WEDEWARDT, C, VOGEL, M, WULFTANGE, H, GELLER, F, STÜBING, K, SIEGFRIED, W, GOLDSCHMIDT, H.-P
Published in The journal of clinical endocrinology and metabolism (01.08.2000)
Published in The journal of clinical endocrinology and metabolism (01.08.2000)
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Evidence for clinical and genetic heterogeneity of syndactyly type I: the phenotype of second and third toe syndactyly maps to chromosome 3p21.31
MALIK, Sajid, SCHOTT, Jörg, WAJAHAT ALI, Syed, OEFFNER, Frank, AMIN-UD-DIN, Muhammad, AHMAD, Wasim, GRZESCHIK, Karl-Heinz, KOCH, Manuela C
Published in European journal of human genetics : EJHG (01.12.2005)
Published in European journal of human genetics : EJHG (01.12.2005)
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Journal Article
Lisch corneal dystrophy is genetically distinct from Meesmann corneal dystrophy and maps to Xp22.3
Lisch, Walter, Büttner, Andreas, Oeffner, Frank, Böddeker, Inke, Engel, Hartmut, Lisch, Christina, Ziegler, Andreas, Grzeschik, Karl-Heinz
Published in American journal of ophthalmology (01.10.2000)
Published in American journal of ophthalmology (01.10.2000)
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A novel type of autosomal recessive syndactyly: Clinical and molecular studies in a family of Pakistani origin
Malik, Sajid, Arshad, Muhammad, Amin-ud-Din, Muhammad, Oeffner, Frank, Dempfle, Astrid, Haque, Sayedul, Koch, Manuela C., Ahmad, Wasim, Grzeschik, Karl-Heinz
Published in American journal of medical genetics. Part A (01.04.2004)
Published in American journal of medical genetics. Part A (01.04.2004)
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Journal Article
Primary meningioma of the optical nerve sheet in infancy as initial presentation of neurofibromatosis type 2
Theurer, S, Biewald, E, Kuchelmeister, K, Temming, P, Kuechler, A, Oeffner, F, Bornfeld, N, Sirin, S, Schmid, K W, Metz, K
Published in Der Pathologe (01.03.2019)
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Published in Der Pathologe (01.03.2019)
Journal Article
Rothmund-Thomson syndrome type 1 caused by biallelic ANAPC1 gene mutations
Zirn, B, Bernbeck, U, Alt, K, Oeffner, F, Gerhardinger, A, Has, C
Published in Skin health and disease (01.03.2021)
Published in Skin health and disease (01.03.2021)
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Primäres Meningeom des Nervus opticus im Säuglingsalter als Erstmanifestation einer Neurofibromatose Typ 2
Theurer, S., Biewald, E., Kuchelmeister, K., Temming, P., Kuechler, A., Oeffner, F., Bornfeld, N., Sirin, S., Schmid, K. W., Metz, K.
Published in Der Pathologe (01.03.2019)
Published in Der Pathologe (01.03.2019)
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Journal Article
Primary meningioma of the optical nerve sheet in infancy as initial presentation of neurofibromatosis type 2
Theurer, S, Biewald, E, Kuchelmeister, K, Temming, P, Kuechler, A, Oeffner, F, Bornfeld, N, Sirin, S, Schmid, K W, Metz, K
Published in Der Pathologe (01.03.2019)
Published in Der Pathologe (01.03.2019)
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Journal Article
Nuclear translocation of mutagenized forms of human cytomegalovirus glycoprotein B (gpUL55)
Bogner, E, Anheier, B, Offner, F, Smuda, C, Reschke, M, Eickmann, M, Radsak, K
Published in Journal of general virology (01.07.1997)
Published in Journal of general virology (01.07.1997)
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