Items where Author is "Hoopmann, Markus"

Article

Geis, Tobias and Roedl, Tanja and Topaloglu, Haluk and Balci-Hayta, Burcu and Hinreiner, Sophie and Mueller-Felber, Wolfgang and Schoser, Benedikt and Mehraein, Yasmin and Huebner, Angela and Zirn, Birgit and Hoopmann, Markus and Reutter, Heiko and Mowat, David and Schuierer, Gerhard and Schara, Ulrike and Hehr, Ute and Koelbel, Heike (2019) Clinical long-time course, novel mutations and genotype-phenotype correlation in a cohort of 27 families with POMT1-related disorders. ORPHANET JOURNAL OF RARE DISEASES, 14: 179. ISSN 1750-1172

Ebenrett, I. and Koerber, F. and Gabriel, H. and Hehr, U. and Heller, R. and Hoopmann, Markus (2009) Targeted Genetic Diagnosis After First Trimester Ultrasound for Lethal Fetal Skeletal Dysplasia. GEBURTSHILFE UND FRAUENHEILKUNDE, 69 (3). pp. 244-247. ISSN 0016-5751, 1438-8804

Michalk, Anne and Stricker, Sigmar and Becker, Jutta and Rupps, Rosemarie and Pantzar, Tapio and Miertus, Jan and Botta, Giovanni and Naretto, Valeria G. and Janetzki, Catrin and Yaqoob, Nausheen and Ott, Claus-Eric and Seelow, Dominik and Wieczorek, Dagmar and Fiebig, Britta and Wirth, Brunhilde and Hoopmann, Markus and Walther, Marisa and Koerber, Friederike and Blankenburg, Markus and Mundlos, Stefan and Heller, Raoul and Hoffmann, Katrin (2008) Acetylcholine receptor pathway mutations explain various fetal akinesia deformation sequence disorders. AMERICAN JOURNAL OF HUMAN GENETICS, 82 (2). pp. 464-476. ISSN 0002-9297, 1537-6605