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Matthew A Lines

Showing results (1-10 of 37) with videos related to

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CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|May 12, 2004
Genetics and ARMDIan M MacDonald, Matthew A Lines
Human Molecular Genetics|May 17, 2002
Molecular genetics of Axenfeld-Rieger malformationsMatthew A Lines, Kathy Kozlowski, Michael A Walter
BMC Pediatrics|April 22, 2020
Autosomal dominant transmission of transient neonatal lactic acidosis: a case reportEmily B Mardian, Matthew A Lines, , et al.
American Journal of Respiratory and Critical Care Medicine|March 18, 2014
Novel mutation in ABCA3 resulting in fatal congenital surfactant deficiency in two siblingsGregory P Moore, Matthew A Lines, Michael T Geraghty, et al.
Ophthalmology|October 3, 2002
Electrophysiologic and phenotypic features of an autosomal cone-rod dystrophy caused by a novel CRX mutationMatthew A Lines, Marc Hébert, Kerry E McTaggart, et al.
Neurology. Genetics|July 2, 2020
A splice variant in <i>ATAD3A</i> expands the clinical and genetic spectrum of Harel-Yoon syndromeIlana Hanes, Hugh J McMillan, Yoko Ito, et al.
Scientific Reports|November 24, 2021
A new automated tool to quantify nucleoid distribution within mitochondrial networksHema Saranya Ilamathi, Mathieu Ouellet, Rasha Sabouny, et al.
JIMD Reports|November 14, 2013
Danon Disease Due to a Novel LAMP2 MicroduplicationMatthew A Lines, Stacy Hewson, William Halliday, et al.
Human Molecular Genetics|February 2, 2006
Functional interactions between FOXC1 and PITX2 underlie the sensitivity to FOXC1 gene dose in Axenfeld-Rieger syndrome and anterior segment dysgenesisFred B Berry, Matthew A Lines, J Martin Oas, et al.
American Journal of Medical Genetics. Part A|June 12, 2021
PHKA2 variants expand the phenotype of phosphorylase B kinase deficiency to include patients with ketotic hypoglycemia onlyAnne Benner, Yazeid Alhaidan, Matthew A Lines, et al.
Pageof 4

Showing results (1-10 of 37) with videos related to

Sort By:
Pageof 4
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|May 12, 2004
Genetics and ARMDIan M MacDonald, Matthew A Lines
Human Molecular Genetics|May 17, 2002
Molecular genetics of Axenfeld-Rieger malformationsMatthew A Lines, Kathy Kozlowski, Michael A Walter
BMC Pediatrics|April 22, 2020
Autosomal dominant transmission of transient neonatal lactic acidosis: a case reportEmily B Mardian, Matthew A Lines, , et al.
American Journal of Respiratory and Critical Care Medicine|March 18, 2014
Novel mutation in ABCA3 resulting in fatal congenital surfactant deficiency in two siblingsGregory P Moore, Matthew A Lines, Michael T Geraghty, et al.
Ophthalmology|October 3, 2002
Electrophysiologic and phenotypic features of an autosomal cone-rod dystrophy caused by a novel CRX mutationMatthew A Lines, Marc Hébert, Kerry E McTaggart, et al.
Neurology. Genetics|July 2, 2020
A splice variant in <i>ATAD3A</i> expands the clinical and genetic spectrum of Harel-Yoon syndromeIlana Hanes, Hugh J McMillan, Yoko Ito, et al.
Scientific Reports|November 24, 2021
A new automated tool to quantify nucleoid distribution within mitochondrial networksHema Saranya Ilamathi, Mathieu Ouellet, Rasha Sabouny, et al.
JIMD Reports|November 14, 2013
Danon Disease Due to a Novel LAMP2 MicroduplicationMatthew A Lines, Stacy Hewson, William Halliday, et al.
Human Molecular Genetics|February 2, 2006
Functional interactions between FOXC1 and PITX2 underlie the sensitivity to FOXC1 gene dose in Axenfeld-Rieger syndrome and anterior segment dysgenesisFred B Berry, Matthew A Lines, J Martin Oas, et al.
American Journal of Medical Genetics. Part A|June 12, 2021
PHKA2 variants expand the phenotype of phosphorylase B kinase deficiency to include patients with ketotic hypoglycemia onlyAnne Benner, Yazeid Alhaidan, Matthew A Lines, et al.
Pageof 4