Killing the messenger: new insights into nonsense-mediated mRNA decay

著者: Byers, Peter H.
出版事項 2002

Determination of the molecular basis of Marfan syndrome: a growth industry

著者: Byers, Peter H.
出版事項 2004

Reply to Jenkins

著者: Byers, Peter H.
出版事項 2000

A Look Back

著者: Byers, Peter H.
出版事項 1999

If Only We Spoke the Same Language—We Would Have So Much to Discuss

著者: Byers, Peter H.
出版事項 2006

Introductory Speech for Joseph D. McInerney

著者: Byers, Peter H.
出版事項 2006

Editorial: Bells and whistles

著者: Byers, Peter H.
出版事項 1997

Molecular Genetic Pathology : Coming of Age in the Molecular World

著者: Byers, Peter H.
出版事項 1999

Molecular Genetic Pathology: Coming of Age in the Molecular World

著者: Byers, Peter H.
出版事項 1999

The Next Five Years

著者: Byers, Peter H.
出版事項 1994

Production of Procollagen by Human Fibroblasts in Culture

著者: Smith, Barbara D., Byers, Peter H., Martin, George R.
出版事項 1972

Genetic evaluation of suspected osteogenesis imperfecta (OI)

著者: Byers, Peter H., Krakow, Deborah, Nunes, Mark E., Pepin, Melanie
出版事項 2006

Molecular Mechanisms of Classical Ehlers-Danlos Syndrome

著者: Mitchell, Anna L., Schwarze, Ulrike, Jennings, Jessica F., Byers, Peter H.
出版事項 2009

6q25.1 (TAB2) microdeletion is a risk factor for hypoplastic left heart: a case report that expands the phenotype

著者: Cheng, Andrew, Neufeld-Kaiser, Whitney, Byers, Peter H., Liu, Yajuan J.
出版年 BMC Cardiovasc Disord (2020)

A Homozygous B3GAT3 Mutation Causes a Severe Syndrome with Multiple Fractures, Extending the Number of Linkeropathy Syndromes

著者: Jones, Kelly L., Schwarze, Ulrike, Adam, Margaret P., Byers, Peter H., Mefford, Heather C.
出版年 Am J Med Genet A (2015)

Extrathoracic subclavian artery aneurysm in a patient with suspected genetic arteriopathy

著者: Banning, Stephanie K., Ur, Rebecca, Malleis, James, Hamlat, Christian A., Byers, Peter H., Shalhub, Sherene
出版年 J Vasc Surg Cases Innov Tech (2020)

Allelic background of LEPRE1 mutations that cause recessive forms of osteogenesis imperfecta in different populations

著者: Pepin, Melanie G, Schwarze, Ulrike, Singh, Virendra, Romana, Marc, Jones-LeCointe, Altheia, Byers, Peter H
出版事項 2013

Order of Intron Removal Influences Multiple Splice Outcomes, Including a Two-Exon Skip, in a COL5A1 Acceptor-Site Mutation That Results in Abnormal Pro-α1(V) N-Propeptides and Ehle...

著者: Takahara, Kazuhiko, Schwarze, Ulrike, Imamura, Yasutada, Hoffman, Guy G., Toriello, Helga, Smith, Lynne T., Byers, Peter H., Greenspan, Daniel S.
出版事項 2002

Gene Targeting of Mutant COL1A2 Alleles in Mesenchymal Stem Cells From Individuals With Osteogenesis Imperfecta

著者: Chamberlain, Joel R, Deyle, David R, Schwarze, Ulrike, Wang, Peirong, Hirata, Yi Li, Byers, Peter H, Russell, David W
出版事項 2007

Rare Autosomal Recessive Cardiac Valvular Form of Ehlers-Danlos Syndrome Results from Mutations in the COL1A2 Gene That Activate the Nonsense-Mediated RNA Decay Pathway

著者: Schwarze, Ulrike, Hata, Ryu-Ichiro, McKusick, Victor A., Shinkai, Hiroshi, Hoyme, H. Eugene, Pyeritz, Reed E., Byers, Peter H.
出版事項 2004