Items where Author is "Martin, Peter"

Article

Kortuem, Fanny and Das, Soma and Flindt, Max and Morris-Rosendahl, Deborah J. and Stefanova, Irina and Goldstein, Amy and Horn, Denise and Klopocki, Eva and Kluger, Gerhard and Martin, Peter and Rauch, Anita and Roumer, Agathe and Saitta, Sulagna and Walsh, Laurence E. and Wieczorek, Dagmar and Uyanik, Goekhan and Kutsche, Kerstin and Dobyns, William B. (2011) The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis. JOURNAL OF MEDICAL GENETICS, 48 (6). pp. 396-406. ISSN 0022-2593

Martin, Peter and Uyanik, Gökhan and Wiemer-Kruel, Adelheid and Schneider, Silvia and Gross, Claudia and Hehr, Ute and Winkler, Jürgen (2004) Different clinical and morphological phenotypes in monozygotic twins with identical DCX mutation. JOURNAL OF NEUROLOGY, 251 (1). pp. 108-110. ISSN 0340-5354