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Mutation Research|February 13, 2001
Mutation frequency is reduced in the cerebellum of Big Blue mice overexpressing a human wild type SOD1 geneM Kunishige, K A Hill, A M Riemer, et al.
The British Journal of Dermatology|August 14, 2002
Type-IV hypersensitivity to betamethasone valerate and clobetasol propionate: results of a multicentre studyS Sommer, S M Wilkinson, J S C English, et al.
Nature|August 15, 2003
In situ experimental evidence of the fate of a phytodetritus pulse at the abyssal sea floorU Witte, F Wenzhöfer, S Sommer, et al.
Human Molecular Genetics|April 1, 1995
The D5 dopamine receptor gene in schizophrenia: identification of a nonsense change and multiple missense changes but lack of association with diseaseJ L Sobell, T J Lind, D C Sigurdson, et al.
Neuroscience Letters|September 21, 2010
Identification of high risk DISC1 protein structural variants in patients with bipolar spectrum disorderWenjia Song, Wenyan Li, Katie Noltner, et al.
Molecular Ecology|July 1, 2014
Invasion genetics of a human commensal rodent: the black rat Rattus rattus in MadagascarC Brouat, C Tollenaere, A Estoup, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|June 24, 2004
MECP2 structural and 3'-UTR variants in schizophrenia, autism and other psychiatric diseases: a possible association with autismAkane Shibayama, Edwin H Cook, Jinong Feng, et al.
British Journal of Haematology|June 1, 1990
A past mutation at isoleucine 397 is now a common cause of moderate/mild haemophilia BC D Bottema, D D Koeberl, R P Ketterling, et al.
Biotechniques|May 25, 1999
Detection of virtually all mutations-SSCP (DOVAM-S): a rapid method for mutation scanning with virtually 100% sensitivityQ Liu, J Feng, C Buzin, et al.
Genomics|September 19, 1998
Blind analysis of denaturing high-performance liquid chromatography as a tool for mutation detectionM C O'Donovan, P J Oefner, S C Roberts, et al.
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