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Peter H Byers

Showing results (11-20 of 102) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 13, 2014
Pregnancy-related deaths and complications in women with vascular Ehlers-Danlos syndromeMitzi L Murray, Melanie Pepin, Suzanne Peterson, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|April 26, 2003
Identification, characterization and expression analysis of a new fibrillar collagen gene, COL27A1James M Pace, Marcella Corrado, Caterina Missero, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 17, 2006
Genetic evaluation of suspected osteogenesis imperfecta (OI)Peter H Byers, Deborah Krakow, Mark E Nunes, et al.
American Journal of Medical Genetics. Part A|March 29, 2014
FKBP14-related Ehlers-Danlos syndrome: expansion of the phenotype to include vascular complicationsMitzi L Murray, Margaret Yang, Christine Fauth, et al.
Human Mutation|April 17, 2009
Molecular mechanisms of classical Ehlers-Danlos syndrome (EDS)Anna L Mitchell, Ulrike Schwarze, Jessica F Jennings, et al.
BMC Cardiovascular Disorders|March 19, 2020
6q25.1 (TAB2) microdeletion is a risk factor for hypoplastic left heart: a case report that expands the phenotypeAndrew Cheng, Whitney Neufeld-Kaiser, Peter H Byers, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 4, 2011
COL3A1 haploinsufficiency results in a variety of Ehlers-Danlos syndrome type IV with delayed onset of complications and longer life expectancyDru F Leistritz, Melanie G Pepin, Ulrike Schwarze, et al.
Journal of Vascular Surgery Cases and Innovative Techniques|September 10, 2021
True radial artery aneurysm in a patient with somatic mosaicism for a mutation in platelet-derived growth factor receptor β geneSherene Shalhub, Lisa Hysa, Peter H Byers, et al.
Journal of Vascular Surgery|March 8, 2018
Testing patterns for genetically triggered aortic and arterial aneurysms and dissections at an academic centerKelli L Hicks, Peter H Byers, Elina Quiroga, et al.
American Journal of Medical Genetics. Part A|June 11, 2019
Compound heterozygosity for a frameshift mutation and an upstream deletion that reduces expression of SERPINH1 in siblings with a moderate form of osteogenesis imperfectaUlrike Schwarze, Tim Cundy, Yajuan J Liu, et al.
Pageof 11

Showing results (11-20 of 102) with videos related to

Sort By:
Pageof 11
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 13, 2014
Pregnancy-related deaths and complications in women with vascular Ehlers-Danlos syndromeMitzi L Murray, Melanie Pepin, Suzanne Peterson, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|April 26, 2003
Identification, characterization and expression analysis of a new fibrillar collagen gene, COL27A1James M Pace, Marcella Corrado, Caterina Missero, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 17, 2006
Genetic evaluation of suspected osteogenesis imperfecta (OI)Peter H Byers, Deborah Krakow, Mark E Nunes, et al.
American Journal of Medical Genetics. Part A|March 29, 2014
FKBP14-related Ehlers-Danlos syndrome: expansion of the phenotype to include vascular complicationsMitzi L Murray, Margaret Yang, Christine Fauth, et al.
Human Mutation|April 17, 2009
Molecular mechanisms of classical Ehlers-Danlos syndrome (EDS)Anna L Mitchell, Ulrike Schwarze, Jessica F Jennings, et al.
BMC Cardiovascular Disorders|March 19, 2020
6q25.1 (TAB2) microdeletion is a risk factor for hypoplastic left heart: a case report that expands the phenotypeAndrew Cheng, Whitney Neufeld-Kaiser, Peter H Byers, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 4, 2011
COL3A1 haploinsufficiency results in a variety of Ehlers-Danlos syndrome type IV with delayed onset of complications and longer life expectancyDru F Leistritz, Melanie G Pepin, Ulrike Schwarze, et al.
Journal of Vascular Surgery Cases and Innovative Techniques|September 10, 2021
True radial artery aneurysm in a patient with somatic mosaicism for a mutation in platelet-derived growth factor receptor β geneSherene Shalhub, Lisa Hysa, Peter H Byers, et al.
Journal of Vascular Surgery|March 8, 2018
Testing patterns for genetically triggered aortic and arterial aneurysms and dissections at an academic centerKelli L Hicks, Peter H Byers, Elina Quiroga, et al.
American Journal of Medical Genetics. Part A|June 11, 2019
Compound heterozygosity for a frameshift mutation and an upstream deletion that reduces expression of SERPINH1 in siblings with a moderate form of osteogenesis imperfectaUlrike Schwarze, Tim Cundy, Yajuan J Liu, et al.
Pageof 11