Benutzerspezifische Werkzeuge

Publikationen - 2014

Zimmermann,K., Gorgens,H., Brauer,D., Einsle,F., Noack,B., von Kannen,S., Grossmann,M., Hoyer,J., Strobel,A., Kollner,V., Weidner,K., Ziegler,A., Hemmelmann,C., and Schackert,H.K. (2014). Analysis of gastrin-releasing peptide gene and gastrin-releasing peptide receptor gene in patients with agoraphobia. Psychiatr. Genet. 24, 232-233.
Steinke,V., Holzapfel,S., Loeffler,M., Holinski-Feder,E., Morak,M., Schackert,H.K., Gorgens,H., Pox,C., Royer-Pokora,B., Knebel-Doeberitz,M., Buttner,R., Propping,P., and Engel,C. (2014). Evaluating the performance of clinical criteria for predicting mismatch repair gene mutations in Lynch syndrome: a comprehensive analysis of 3,671 families. Int. J. Cancer 135, 69-77.
Yang,R., Chen,B., Pfutze,K., Buch,S., Steinke,V., Holinski-Feder,E., Stocker,S., von Schonfels,W., Becker,T., Schackert,H.K., Royer-Pokora,B., Kloor,M., Schmiegel,W.H., Buttner,R., Engel,C., Lascorz,P.J., Forsti,A., Kunkel,N., Bugert,P., Schreiber,S., Krawczak,M., Schafmayer,C., Propping,P., Hampe,J., Hemminki,K., and Burwinkel,B. (2014). Genome-wide analysis associates familial colorectal cancer with increases in copy number variations and a rare structural variation at 12p12.3. Carcinogenesis 35, 315-323.
Schackert,H.K., Agha-Hosseini,F., Gorgens,H., Jatzwauk,M., von Kannen,S., Noack,B., Eckelt,U., Hoffmann,P., Shabestari,S.B., and Mehdipour,P. (2014). Complete homozygous deletion of CTSC in an Iranian family with Papillon-Lefevre syndrome. Int. J. Dermatol. 53, 885-887.