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Page 1
De novo mutations in FOXP1 in cases with intellectual disability, autism, and language impairment.
Hamdan FF, Daoud H, Rochefort D, Piton A, Gauthier J, Langlois M, Foomani G, Dobrzeniecka S, Krebs MO, Joober R, Lafrenière RG, Lacaille JC, Mottron L, Drapeau P, Beauchamp MH, Phillips MS, Fombonne E, Rouleau GA, Michaud JL. Hamdan FF, et al. Among authors: joober r. Am J Hum Genet. 2010 Nov 12;87(5):671-8. doi: 10.1016/j.ajhg.2010.09.017. Epub 2010 Oct 14. Am J Hum Genet. 2010. PMID: 20950788 Free PMC article.
Schizophrenia and chromosome 6p.
Turecki G, Rouleau GA, Joober R, Mari J, Morgan K. Turecki G, et al. Among authors: joober r. Am J Med Genet. 1997 Apr 18;74(2):195-8. Am J Med Genet. 1997. PMID: 9129723 Review.
Analysis of 14 CAG repeat-containing genes in schizophrenia.
Joober R, Benkelfat C, Toulouse A, Lafrenière RG, Lal S, Ajroud S, Turecki G, Bloom D, Labelle A, Lalonde P, Alda M, Morgan K, Palmour R, Rouleau GA. Joober R, et al. Am J Med Genet. 1999 Dec 15;88(6):694-9. Am J Med Genet. 1999. PMID: 10581491
Polymorphism in the cell division cycle 45 like gene and schizophrenia.
Yamamoto K, Bloom D, La S, Turecki G, Joober R, Benkelfat C, Lalonde P, Labelle A, Rouleau GA. Yamamoto K, et al. Among authors: joober r. Am J Med Genet. 2001 Mar 8;105(2):214-5. doi: 10.1002/ajmg.1198. Am J Med Genet. 2001. PMID: 11304839 No abstract available.
448 results