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Interchromosomal template-switching as a novel molecular mechanism for imprinting perturbations associated with Temple syndrome.
Carvalho, Claudia M B; Coban-Akdemir, Zeynep; Hijazi, Hadia; Yuan, Bo; Pendleton, Matthew; Harrington, Eoghan; Beaulaurier, John; Juul, Sissel; Turner, Daniel J; Kanchi, Rupa S; Jhangiani, Shalini N; Muzny, Donna M; Gibbs, Richard A; Stankiewicz, Pawel; Belmont, John W; Shaw, Chad A; Cheung, Sau Wai; Hanchard, Neil A; Sutton, V Reid; Bader, Patricia I; Lupski, James R.
Afiliação
  • Carvalho CMB; Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, Room 604B, Houston, TX, 77030-3498, USA. cfonseca@bcm.edu.
  • Coban-Akdemir Z; Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, Room 604B, Houston, TX, 77030-3498, USA.
  • Hijazi H; Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, Room 604B, Houston, TX, 77030-3498, USA.
  • Yuan B; Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, Room 604B, Houston, TX, 77030-3498, USA.
  • Pendleton M; Oxford Nanopore Technologies Inc, New York, NY, USA.
  • Harrington E; Oxford Nanopore Technologies Inc, New York, NY, USA.
  • Beaulaurier J; Oxford Nanopore Technologies Inc, San Francisco, CA, USA.
  • Juul S; Oxford Nanopore Technologies Inc, New York, NY, USA.
  • Turner DJ; Oxford Nanopore Technologies Inc, San Francisco, CA, USA.
  • Kanchi RS; Oxford Nanopore Technologies Ltd, Oxford, UK.
  • Jhangiani SN; UT MD Anderson Cancer Center, Houston, TX, USA.
  • Muzny DM; Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX, 77030, USA.
  • Gibbs RA; Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX, 77030, USA.
  • Stankiewicz P; Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX, 77030, USA.
  • Shaw CA; Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, Room 604B, Houston, TX, 77030-3498, USA.
  • Cheung SW; Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, Room 604B, Houston, TX, 77030-3498, USA.
  • Hanchard NA; Department of Pediatrics, Baylor College of Medicine, Houston, TX, 77030, USA.
  • Sutton VR; Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, Room 604B, Houston, TX, 77030-3498, USA.
  • Bader PI; Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, Room 604B, Houston, TX, 77030-3498, USA.
  • Lupski JR; Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, Room 604B, Houston, TX, 77030-3498, USA.
Genome Med ; 11(1): 25, 2019 04 23.
Article em En | MEDLINE | ID: mdl-31014393
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 14 / Aberrações Cromossômicas / Impressão Genômica / Transtornos Cromossômicos Tipo de estudo: Risk_factors_studies Limite: Adult / Humans / Male Idioma: En Revista: Genome Med Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Reino Unido
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 14 / Aberrações Cromossômicas / Impressão Genômica / Transtornos Cromossômicos Tipo de estudo: Risk_factors_studies Limite: Adult / Humans / Male Idioma: En Revista: Genome Med Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Reino Unido