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About this nonfiction
The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis by Fanny Kortüm, Soma Das, Max Flindt, Deborah J Morris-Rosendahl, Irina Stefanova, Amy Goldstein, Denise Horn, Eva Klopocki, Gerhard Kluger, Peter Martin, Anita Rauch, Agathe Roumer, Sulagna Saitta, Laurence E Walsh, Dagmar Wieczorek, Gökhan Uyanik, Kerstin Kutsche, William B Dobyns is a nonfiction available to read on EtoBox.
It is typically read by self-directed learners exploring a subject in depth.
Common subject areas: history, science, philosophy, social sciences.
- Author
- Fanny Kortüm, Soma Das, Max Flindt, Deborah J Morris-Rosendahl, Irina Stefanova, Amy Goldstein, Denise Horn, Eva Klopocki, Gerhard Kluger, Peter Martin, Anita Rauch, Agathe Roumer, Sulagna Saitta, Laurence E Walsh, Dagmar Wieczorek, Gökhan Uyanik, Kerstin Kutsche, William B Dobyns
- Publisher
- BMJ Publishing Group
- Published
- 2011
- Language
- EN
- Category
- nonfiction