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Consistency of variant interpretations among bioinformaticians and clinical geneticists in hereditary cancer panels.
Agaoglu, Nihat Bugra; Unal, Busra; Akgun Dogan, Ozlem; Kanev, Martin Orlinov; Zolfagharian, Payam; Ozemri Sag, Sebnem; Temel, Sehime Gulsun; Doganay, Levent.
Afiliación
  • Agaoglu NB; Department of Medical Genetics, Umraniye Training and Research Hospital, University of Health Sciences, Istanbul, Turkey. nbagaoglu@hotmail.com.
  • Unal B; Genomic Laboratory (GLAB), Umraniye Training and Research Hospital, University of Health Sciences, Istanbul, Turkey. nbagaoglu@hotmail.com.
  • Akgun Dogan O; Department of Medical Genetics, Umraniye Training and Research Hospital, University of Health Sciences, Istanbul, Turkey.
  • Kanev MO; Genomic Laboratory (GLAB), Umraniye Training and Research Hospital, University of Health Sciences, Istanbul, Turkey.
  • Zolfagharian P; Genomic Laboratory (GLAB), Umraniye Training and Research Hospital, University of Health Sciences, Istanbul, Turkey.
  • Ozemri Sag S; Department of Pediatric Genetics, Umraniye Training and Research Hospital, University of Health Sciences, Istanbul, Turkey.
  • Temel SG; Department of Biotechnology and Genetic, Institute of Science, Trakya University, Edirne, Turkey.
  • Doganay L; Genomic Laboratory (GLAB), Umraniye Training and Research Hospital, University of Health Sciences, Istanbul, Turkey.
Eur J Hum Genet ; 30(3): 378-383, 2022 03.
Article en En | MEDLINE | ID: mdl-35132179
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Predisposición Genética a la Enfermedad / Neoplasias Tipo de estudio: Guideline Límite: Humans Idioma: En Revista: Eur J Hum Genet Asunto de la revista: GENETICA MEDICA Año: 2022 Tipo del documento: Article País de afiliación: Turquía Pais de publicación: Reino Unido
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Predisposición Genética a la Enfermedad / Neoplasias Tipo de estudio: Guideline Límite: Humans Idioma: En Revista: Eur J Hum Genet Asunto de la revista: GENETICA MEDICA Año: 2022 Tipo del documento: Article País de afiliación: Turquía Pais de publicación: Reino Unido