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Neuroscience Letters|May 25, 2010
Genetic variation of CHRNA4 does not modulate attention in Parkinson's diseaseGavin Hudson, Andrea Stutt, Martin Eccles, et al.
Nature Genetics|May 10, 2000
Mutations in TFAP2B cause Char syndrome, a familial form of patent ductus arteriosusM Satoda, F Zhao, G A Diaz, et al.
Journal of Medical Genetics|December 1, 1990
Alagille syndrome and deletion of 20pF Anad, J Burn, D Matthews, et al.
Brain : a Journal of Neurology|June 16, 2001
The prevalence of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome) in the UKU Nath, Y Ben-Shlomo, R G Thomson, et al.
Acta Gastro-Enterologica Belgica|September 1, 1995
The genetic background of familial adenomatous polyposis. Linkage analysis, the APC gene identification and mutation screeningA Kartheuser, S West, C Walon, et al.
International Journal of Geriatric Psychiatry|August 15, 2006
Orthostatic hypotension in Parkinson's disease: association with cognitive decline?Liesl M Allcock, Rose Anne Kenny, Urs Peter Mosimann, et al.
American Journal of Human Genetics|November 1, 1992
Molecular genetic study of the frequency of monosomy 22q11 in DiGeorge syndromeA H Carey, D Kelly, S Halford, et al.
International Journal of Geriatric Psychiatry|July 22, 2006
Cholinesterase inhibitors in advanced Dementia with Lewy bodies: increase or stop?Sanjeet Pakrasi, Alan Thomas, Urs P Mosimann, et al.
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