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M Forrest

Showing results (311-320 of 343) with videos related to

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American Journal of Medical Genetics|October 26, 1999
Clinical and genetic study of Friedreich ataxia in an Australian populationM B Delatycki, D B Paris, R J Gardner, et al.
Neurobiology of Disease|June 28, 2003
Spinocerebellar ataxia type 15 (sca15) maps to 3p24.2-3pter: exclusion of the ITPR1 gene, the human orthologue of an ataxic mouse mutantMelanie A Knight, Marina L Kennerson, Richard J Anney, et al.
Cancer Radiotherapie : Journal De La Societe Francaise De Radiotherapie Oncologique|September 2, 2008
[Experience feed back committee in radiotherapy (CREx): a compulsory tool for security management evaluation at two years]E Lartigau, B Coche-Dequeant, V Dumortier, et al.
Lancet (London, England)|December 5, 1987
Effective strategy for prenatal prediction of Duchenne and Becker muscular dystrophyS M Forrest, T J Smith, G S Cross, et al.
Neuroreport|April 20, 1999
Early-onset Alzheimer's disease caused by a novel mutation at codon 219 of the presenilin-1 geneM J Smith, R J Gardner, M A Knight, et al.
The Journal of General Virology|September 1, 1990
Sulphoevernan, a polyanionic polysaccharide, and the narcissus lectin potently inhibit human immunodeficiency virus infection by binding to viral envelope proteinB E Weiler, H C Schröder, V Stefanovich, et al.
American Journal of Medical Genetics|September 1, 1990
Characterization of deletions in the dystrophin gene giving mild phenotypesD R Love, T J Flint, R F Marsden, et al.
Research Communications in Molecular Pathology and Pharmacology|July 2, 2002
Levels of lipid peroxidation products in a chronic inflammatory disorderC L Deaney, K Feyi, C M Forrest, et al.
Pediatric Dermatology|March 24, 2020
Recurrent sterile abscesses in a case of X-linked neutropeniaCatherine M Biggs, Bhavi Modi, Michelle Steinraths, et al.
Nature|January 11, 1990
Very mild muscular dystrophy associated with the deletion of 46% of dystrophinS B England, L V Nicholson, M A Johnson, et al.
Pageof 35

Showing results (311-320 of 343) with videos related to

Sort By:
Pageof 35
American Journal of Medical Genetics|October 26, 1999
Clinical and genetic study of Friedreich ataxia in an Australian populationM B Delatycki, D B Paris, R J Gardner, et al.
Neurobiology of Disease|June 28, 2003
Spinocerebellar ataxia type 15 (sca15) maps to 3p24.2-3pter: exclusion of the ITPR1 gene, the human orthologue of an ataxic mouse mutantMelanie A Knight, Marina L Kennerson, Richard J Anney, et al.
Cancer Radiotherapie : Journal De La Societe Francaise De Radiotherapie Oncologique|September 2, 2008
[Experience feed back committee in radiotherapy (CREx): a compulsory tool for security management evaluation at two years]E Lartigau, B Coche-Dequeant, V Dumortier, et al.
Lancet (London, England)|December 5, 1987
Effective strategy for prenatal prediction of Duchenne and Becker muscular dystrophyS M Forrest, T J Smith, G S Cross, et al.
Neuroreport|April 20, 1999
Early-onset Alzheimer's disease caused by a novel mutation at codon 219 of the presenilin-1 geneM J Smith, R J Gardner, M A Knight, et al.
The Journal of General Virology|September 1, 1990
Sulphoevernan, a polyanionic polysaccharide, and the narcissus lectin potently inhibit human immunodeficiency virus infection by binding to viral envelope proteinB E Weiler, H C Schröder, V Stefanovich, et al.
American Journal of Medical Genetics|September 1, 1990
Characterization of deletions in the dystrophin gene giving mild phenotypesD R Love, T J Flint, R F Marsden, et al.
Research Communications in Molecular Pathology and Pharmacology|July 2, 2002
Levels of lipid peroxidation products in a chronic inflammatory disorderC L Deaney, K Feyi, C M Forrest, et al.
Pediatric Dermatology|March 24, 2020
Recurrent sterile abscesses in a case of X-linked neutropeniaCatherine M Biggs, Bhavi Modi, Michelle Steinraths, et al.
Nature|January 11, 1990
Very mild muscular dystrophy associated with the deletion of 46% of dystrophinS B England, L V Nicholson, M A Johnson, et al.
Pageof 35