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Cell|May 19, 1995
beta-Amyloid precursor protein-deficient mice show reactive gliosis and decreased locomotor activityH Zheng, M Jiang, M E Trumbauer, et al.
Journal of Medical Genetics|September 23, 2008
Clinical experience in the evaluation of 30 patients with a prior diagnosis of FG syndromeM J Lyons, J M Graham, G Neri, et al.
Human Molecular Genetics|January 15, 1999
The spectrum of mutations in UBE3A causing Angelman syndromeP Fang, E Lev-Lehman, T F Tsai, et al.
Clinical Genetics|August 2, 2011
Ehlers-Danlos arthrochalasia type (VIIA-B)--expanding the phenotype: from prenatal life through adulthoodM Klaassens, E Reinstein, Y Hilhorst-Hofstee, et al.
Communicable Diseases Intelligence Quarterly Report|July 4, 2001
Murray Valley encephalitis virus surveillance and control initiatives in Australia. National Arbovirus Advisory Committee of the Communicable Diseases Network AustraliaJ D Spencer, J Azoulas, A K Broom, et al.
The Journal of Pharmacology and Experimental Therapeutics|September 29, 2004
Dynamics of {beta}-amyloid reductions in brain, cerebrospinal fluid, and plasma of {beta}-amyloid precursor protein transgenic mice treated with a {gamma}-secretase inhibitorD M Barten, V L Guss, J A Corsa, et al.
Human Genetics|November 10, 2001
Scanning for telomeric deletions and duplications and uniparental disomy using genetic markers in 120 children with malformationsM J Rosenberg, C Killoran, L Dziadzio, et al.
The Journal of Infectious Diseases|May 8, 2012
Characteristics of a widespread community cluster of H275Y oseltamivir-resistant A(H1N1)pdm09 influenza in AustraliaA C Hurt, K Hardie, N J Wilson, et al.
Emerging Infectious Diseases|August 4, 2001
Emerging viral diseases of Southeast Asia and the Western PacificJ S Mackenzie, K B Chua, P W Daniels, et al.
Human Molecular Genetics|July 13, 1999
PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndromeD J Marsh, J B Kum, K L Lunetta, et al.
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