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Correction: SMAD6 variants in craniosynostosis: genotype and phenotype evaluation.
Calpena, Eduardo; Cuellar, Araceli; Bala, Krithi; Swagemakers, Sigrid M A; Koelling, Nils; McGowan, Simon J; Phipps, Julie M; Balasubramanian, Meena; Cunningham, Michael L; Douzgou, Sofia; Lattanzi, Wanda; Morton, Jenny E V; Shears, Deborah; Weber, Astrid; Wilson, Louise C; Lord, Helen; Lester, Tracy; Johnson, David; Wall, Steven A; Twigg, Stephen R F; Mathijssen, Irene M J; Boardman-Pretty, Freya; Boyadjiev, Simeon A; Wilkie, Andrew O M.
Afiliación
  • Calpena E; MRCWeatherall Institute of MolecularMedicine, University of Oxford, John Radcliffe Hospital, Oxford, UK.
  • Cuellar A; Department of Pediatrics, University of California-Davis, Sacramento, CA, USA.
  • Bala K; Department of Pediatrics, University of California-Davis, Sacramento, CA, USA.
  • Swagemakers SMA; Departments of Pathology and Bioinformatics, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands.
  • Koelling N; MRCWeatherall Institute of MolecularMedicine, University of Oxford, John Radcliffe Hospital, Oxford, UK.
  • McGowan SJ; MRCWeatherall Institute of MolecularMedicine, University of Oxford, John Radcliffe Hospital, Oxford, UK.
  • Phipps JM; MRCWeatherall Institute of MolecularMedicine, University of Oxford, John Radcliffe Hospital, Oxford, UK.
  • Balasubramanian M; Sheffield Clinical Genetics Service, Sheffield Children's NHS Foundation Trust, Sheffield, UK.
  • Cunningham ML; Division of Craniofacial Medicine, Department of Pediatrics, University of Washington, Seattle, WA, USA.
  • Douzgou S; Manchester Centre for Genomic Medicine, Central Manchester University Hospitals NHS Foundation Trust, Saint Mary's Hospital, Manchester, UK.
  • Lattanzi W; Division of Evolution and Genomic Sciences, School of Biological Sciences, Faculty of Biology, Medicines and Health, University of Manchester, Manchester, UK.
  • Morton JEV; Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.
  • Shears D; Department of Life Science and Public Health, Università Cattolica del Sacro Cuore, Rome, Italy.
  • Weber A; West Midlands Regional Clinical Genetics Service and Birmingham Health Partners, Birmingham Women's and Children's Hospitals NHS Foundation Trust, Birmingham, UK.
  • Wilson LC; Oxford Centre for Genomic Medicine, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
  • Lord H; Craniofacial Unit, Oxford University Hospitals NHS Trust, John Radcliffe Hospital, Oxford, UK.
  • Lester T; Department of Clinical Genetics, Liverpool Women's NHS Foundation Trust, Liverpool, UK.
  • Johnson D; Clinical Genetics Service, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
  • Wall SA; Oxford Genetics Laboratories, Oxford University Hospitals NHS Foundation Trust, The Churchill Hospital, Oxford, UK.
  • Twigg SRF; Oxford Genetics Laboratories, Oxford University Hospitals NHS Foundation Trust, The Churchill Hospital, Oxford, UK.
  • Mathijssen IMJ; Craniofacial Unit, Oxford University Hospitals NHS Trust, John Radcliffe Hospital, Oxford, UK.
  • Boardman-Pretty F; Craniofacial Unit, Oxford University Hospitals NHS Trust, John Radcliffe Hospital, Oxford, UK.
  • Boyadjiev SA; Department of Plastic and Reconstructive Surgery and Hand Surgery, Erasmus MC, University Medical Center Rotterdam, Rotterdam, the Netherlands.
  • Wilkie AOM; Genomics England, London, UK.
Genet Med ; 22(9): 1567, 2020 Sep.
Article en En | MEDLINE | ID: mdl-32636483
ABSTRACT
An amendment to this paper has been published and can be accessed via a link at the top of the paper.
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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Genet Med Asunto de la revista: GENETICA MEDICA Año: 2020 Tipo del documento: Article País de afiliación: Reino Unido
Texto completo
Añadir a Mi BVS
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XML
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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Genet Med Asunto de la revista: GENETICA MEDICA Año: 2020 Tipo del documento: Article País de afiliación: Reino Unido