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Browsing by Author Galli, L

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	Title	Author(s)	Issue Date
	MECP2 mutation in male patients with non-specific X-linked mental retardation Journal:FEBS Letters	Orrico, A Lam, CW Galli, L Dotti, MT Hayek, G Tong, SF Poon, PMK Zappella, M Federico, A Sorrentino, V	2000
	Mutations in the glucose-6-phosphate transporter (G6PT) gene in patients with glycogen storage diseases type 1b and 1c Journal:FEBS Letters	Galli, L Orrico, A Marcolongo, P Fulceri, R Burchell, A Melis, D Parini, R Gatti, R Lam, CW Benedetti, A Sorrentino, V	1999
	Resequencing the G6PT1 gene reveals a novel splicing mutation in a patient with glycogen storage disease type 1b Journal:Clinica Chimica Acta	Lam, CW Orrico, A Yan, MSC Law, TY Galli, L Benedetti, A Tong, SF Sorrentino, V	2006
	A Rett syndrome MECP2 mutation that causes mental retardation in men Journal:Neurology	Dotti, MT Orrico, A De Stefano, N Battisti, C Sicurelli, F Severi, S Lam, CW Galli, L Sorrentino, V Federico, A	2002

Showing results 1 to 4 of 4