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G Lemire

Showing results (31-40 of 47) with videos related to

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Current Genetics|October 1, 1994
Mutations in the structural gene for cytochrome c result in deficiency of both cytochromes aa3 and c in Neurospora crassaD A Bottorff, S Parmaksizoglu, E G Lemire, et al.
Human Mutation|February 16, 2005
Novel mutations and polymorphisms in genes causing hereditary hemorrhagic telangiectasiaSalma A Abdalla, Urszula Cymerman, Diane Rushlow, et al.
American Journal of Surgery|August 1, 1983
Prolene sutures are not a significant factor in anastomotic false aneurysmsM R Gaspar, H J Movius, J J Rosental, et al.
Canadian Respiratory Journal|December 18, 2010
Familial interstitial pulmonary fibrosis: a large family with atypical clinical featuresRanji Chibbar, John A Gjevre, Francis Shih, et al.
American Journal of Medical Genetics|December 2, 1996
A familial disorder with duodenal atresia and tetralogy of FallotE G Lemire, J A Evans, N G Giddins, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|May 11, 2004
Nonspecific interstitial pneumonia and usual interstitial pneumonia with mutation in surfactant protein C in familial pulmonary fibrosisRajni Chibbar, Francis Shih, Monica Baga, et al.
American Journal of Medical Genetics. Part A|September 28, 2016
A novel NDUFS4 frameshift mutation causes Leigh disease in the Hutterite populationRyan E Lamont, Chandree L Beaulieu, Francois P Bernier, et al.
American Journal of Medical Genetics. Part A|April 4, 2017
A de novo deletion in a boy with cerebral palsy suggests a refined critical region for the 4q21.22 microdeletion syndromeMehdi Zarrei, Daniele Merico, Barbara Kellam, et al.
Journal of Pediatric Hematology/Oncology|October 27, 1998
Familial neuroblastoma: report of a kindred with later age at diagnosisE G Lemire, B N Chodirker, G J Williams, et al.
Molecular Genetics & Genomic Medicine|January 24, 2015
Complex genomic rearrangements in the dystrophin gene due to replication-based mechanismsBerivan Baskin, Dimitri J Stavropoulos, Paige A Rebeiro, et al.
Pageof 5

Showing results (31-40 of 47) with videos related to

Sort By:
Pageof 5
Current Genetics|October 1, 1994
Mutations in the structural gene for cytochrome c result in deficiency of both cytochromes aa3 and c in Neurospora crassaD A Bottorff, S Parmaksizoglu, E G Lemire, et al.
Human Mutation|February 16, 2005
Novel mutations and polymorphisms in genes causing hereditary hemorrhagic telangiectasiaSalma A Abdalla, Urszula Cymerman, Diane Rushlow, et al.
American Journal of Surgery|August 1, 1983
Prolene sutures are not a significant factor in anastomotic false aneurysmsM R Gaspar, H J Movius, J J Rosental, et al.
Canadian Respiratory Journal|December 18, 2010
Familial interstitial pulmonary fibrosis: a large family with atypical clinical featuresRanji Chibbar, John A Gjevre, Francis Shih, et al.
American Journal of Medical Genetics|December 2, 1996
A familial disorder with duodenal atresia and tetralogy of FallotE G Lemire, J A Evans, N G Giddins, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|May 11, 2004
Nonspecific interstitial pneumonia and usual interstitial pneumonia with mutation in surfactant protein C in familial pulmonary fibrosisRajni Chibbar, Francis Shih, Monica Baga, et al.
American Journal of Medical Genetics. Part A|September 28, 2016
A novel NDUFS4 frameshift mutation causes Leigh disease in the Hutterite populationRyan E Lamont, Chandree L Beaulieu, Francois P Bernier, et al.
American Journal of Medical Genetics. Part A|April 4, 2017
A de novo deletion in a boy with cerebral palsy suggests a refined critical region for the 4q21.22 microdeletion syndromeMehdi Zarrei, Daniele Merico, Barbara Kellam, et al.
Journal of Pediatric Hematology/Oncology|October 27, 1998
Familial neuroblastoma: report of a kindred with later age at diagnosisE G Lemire, B N Chodirker, G J Williams, et al.
Molecular Genetics & Genomic Medicine|January 24, 2015
Complex genomic rearrangements in the dystrophin gene due to replication-based mechanismsBerivan Baskin, Dimitri J Stavropoulos, Paige A Rebeiro, et al.
Pageof 5