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Browsing by Author Bonin, M.

Full Text	Issue Date	Title	Author(s)
	2011	A two-stage meta-analysis identifies several new loci for Parkinson's disease.	Plagnol, V.; Nalls, M.A.; Bras, J.M.; Hernandez, D.; Sharma, M., et al
	2011	Large deletions of the KCNV2 gene are common in patients with cone dystrophy with supernormal rod response	Wissinger, B.; Schaich, S.; Baumann, B.; Bonin, M.; Jagle, H., et al
	2011	Hybridisation-based resequencing of 17 X-linked intellectual disability genes in 135 patients reveals novel mutations in ATRX, SLC6A8 and PQBP1	Jensen, L.R.; Chen, W.; Moser, B.; Lipkowitz, B.; Schroeder, C., et al
	2009	Molecular karyotyping of patients with unexplained mental retardation by SNP arrays: a multicenter study.	McMullan, D.J.; Bonin, M.; Hehir-Kwa, J.Y.; Vries, L.B.A. de; Dufke, A., et al
	2009	Autosomal dominant spastic paraplegia with peripheral neuropathy maps to chr12q23-24.	Schule, R.; Bonin, M.; Durr, A.; Forlani, S.; Sperfeld, A.D., et al