Author:
Berry-Kravis Elizabeth M.,Lindemann Lothar,Jønch Aia E.,Apostol George,Bear Mark F.,Carpenter Randall L.,Crawley Jacqueline N.,Curie Aurore,Des Portes Vincent,Hossain Farah,Gasparini Fabrizio,Gomez-Mancilla Baltazar,Hessl David,Loth Eva,Scharf Sebastian H.,Wang Paul P.,Von Raison Florian,Hagerman Randi,Spooren Will,Jacquemont Sébastien
Publisher
Springer Science and Business Media LLC
Subject
Drug Discovery,Pharmacology,General Medicine
Reference163 articles.
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3. Handt, M. et al. Point mutation frequency in the FMR1 gene as revealed by fragile X syndrome screening. Mol. Cell Probes 28, 279–283 (2014).
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5. Fisch, G. S. et al. Longitudinal changes in cognitive-behavioral levels in three children with FRAXE. Am. J. Med. Genet. 84, 291–292 (1999).
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