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Janice M Fletcher

Showing results (21-30 of 31) with videos related to

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Ecology Letters|May 15, 2007
Four decades of opposing natural and human-induced artificial selection acting on Windermere pike (Esox lucius)Stephanie M Carlson, Eric Edeline, L Asbjørn Vøllestad, et al.
Proceedings. Biological Sciences|July 30, 2010
Pathogen-induced rapid evolution in a vertebrate life-history traitJan Ohlberger, Øystein Langangen, Eric Edeline, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 28, 2007
Trait changes in a harvested population are driven by a dynamic tug-of-war between natural and harvest selectionEric Edeline, Stephanie M Carlson, Leif C Stige, et al.
Journal of Cellular Physiology|January 27, 2009
Gastrointestinal pathology in a mouse model of mucopolysaccharidosis type IIIAAinslie L K Derrick Roberts, Gordon S Howarth, Wan Chin Liaw, et al.
Annals of Neurology|January 6, 2004
De novo mutations in the mitochondrial ND3 gene as a cause of infantile mitochondrial encephalopathy and complex I deficiencyRobert McFarland, Denise M Kirby, Kerry J Fowler, et al.
NPJ Genomic Medicine|November 23, 2019
Identification and targeted management of a neurodegenerative disorder caused by biallelic mutations in SLC5A6Alicia B Byrne, Peer Arts, Steven W Polyak, et al.
Science Translational Medicine|January 27, 2012
Molecular diagnosis of infantile mitochondrial disease with targeted next-generation sequencingSarah E Calvo, Alison G Compton, Steven G Hershman, et al.
The Australian & New Zealand Journal of Obstetrics & Gynaecology|April 5, 2024
Extending the new era of genomic testing into pregnancy management: A proposed model for Australian prenatal servicesAlice Rogers, Lucas De Jong, Wendy Waters, et al.
JIMD Reports|February 23, 2013
Recommendations on reintroduction of agalsidase Beta for patients with fabry disease in europe, following a period of shortageGabor E Linthorst, Alessandro P Burlina, Franco Cecchi, et al.
Human Mutation|July 13, 2006
Newborn screening for 3-methylcrotonyl-CoA carboxylase deficiency: population heterogeneity of MCCA and MCCB mutations and impact on risk assessmentSonja C Stadler, Roman Polanetz, Esther M Maier, et al.
Pageof 4

Showing results (21-30 of 31) with videos related to

Sort By:
Pageof 4
Ecology Letters|May 15, 2007
Four decades of opposing natural and human-induced artificial selection acting on Windermere pike (Esox lucius)Stephanie M Carlson, Eric Edeline, L Asbjørn Vøllestad, et al.
Proceedings. Biological Sciences|July 30, 2010
Pathogen-induced rapid evolution in a vertebrate life-history traitJan Ohlberger, Øystein Langangen, Eric Edeline, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 28, 2007
Trait changes in a harvested population are driven by a dynamic tug-of-war between natural and harvest selectionEric Edeline, Stephanie M Carlson, Leif C Stige, et al.
Journal of Cellular Physiology|January 27, 2009
Gastrointestinal pathology in a mouse model of mucopolysaccharidosis type IIIAAinslie L K Derrick Roberts, Gordon S Howarth, Wan Chin Liaw, et al.
Annals of Neurology|January 6, 2004
De novo mutations in the mitochondrial ND3 gene as a cause of infantile mitochondrial encephalopathy and complex I deficiencyRobert McFarland, Denise M Kirby, Kerry J Fowler, et al.
NPJ Genomic Medicine|November 23, 2019
Identification and targeted management of a neurodegenerative disorder caused by biallelic mutations in SLC5A6Alicia B Byrne, Peer Arts, Steven W Polyak, et al.
Science Translational Medicine|January 27, 2012
Molecular diagnosis of infantile mitochondrial disease with targeted next-generation sequencingSarah E Calvo, Alison G Compton, Steven G Hershman, et al.
The Australian & New Zealand Journal of Obstetrics & Gynaecology|April 5, 2024
Extending the new era of genomic testing into pregnancy management: A proposed model for Australian prenatal servicesAlice Rogers, Lucas De Jong, Wendy Waters, et al.
JIMD Reports|February 23, 2013
Recommendations on reintroduction of agalsidase Beta for patients with fabry disease in europe, following a period of shortageGabor E Linthorst, Alessandro P Burlina, Franco Cecchi, et al.
Human Mutation|July 13, 2006
Newborn screening for 3-methylcrotonyl-CoA carboxylase deficiency: population heterogeneity of MCCA and MCCB mutations and impact on risk assessmentSonja C Stadler, Roman Polanetz, Esther M Maier, et al.
Pageof 4