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A retrospective analysis of the prevalence of imprinting disorders in Estonia from 1998 to 2016.
Yakoreva, Maria; Kahre, Tiina; Zordania, Riina; Reinson, Karit; Teek, Rita; Tillmann, Vallo; Peet, Aleksandr; Õiglane-Shlik, Eve; Pajusalu, Sander; Murumets, Ülle; Vals, Mari-Anne; Mee, Pille; Wojcik, Monica H; Õunap, Katrin.
Afiliação
  • Yakoreva M; Department of Clinical Genetics, United Laboratories, Tartu University Hospital, Tartu, Estonia.
  • Kahre T; Department of Clinical Genetics, Institute of Clinical Medicine, University of Tartu, Tartu, Estonia.
  • Zordania R; Department of Clinical Genetics, United Laboratories, Tartu University Hospital, Tartu, Estonia.
  • Reinson K; Department of Clinical Genetics, Institute of Clinical Medicine, University of Tartu, Tartu, Estonia.
  • Teek R; Department of Clinical Genetics, United Laboratories, Tartu University Hospital, Tartu, Estonia.
  • Tillmann V; Department of Clinical Genetics, United Laboratories, Tartu University Hospital, Tartu, Estonia.
  • Peet A; Department of Clinical Genetics, Institute of Clinical Medicine, University of Tartu, Tartu, Estonia.
  • Õiglane-Shlik E; Department of Clinical Genetics, United Laboratories, Tartu University Hospital, Tartu, Estonia.
  • Pajusalu S; Department of Paediatrics, Institute of Clinical Medicine, University of Tartu, Tartu, Estonia.
  • Murumets Ü; Children's Clinic, Tartu University Hospital, Tartu, Estonia.
  • Vals MA; Department of Paediatrics, Institute of Clinical Medicine, University of Tartu, Tartu, Estonia.
  • Mee P; Children's Clinic, Tartu University Hospital, Tartu, Estonia.
  • Wojcik MH; Department of Paediatrics, Institute of Clinical Medicine, University of Tartu, Tartu, Estonia.
  • Õunap K; Children's Clinic, Tartu University Hospital, Tartu, Estonia.
Eur J Hum Genet ; 27(11): 1649-1658, 2019 11.
Article em En | MEDLINE | ID: mdl-31186545
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Impressão Genômica / Transtornos Cromossômicos Tipo de estudo: Diagnostic_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Aged80 / Child / Child, preschool / Humans / Infant / Middle aged / Newborn País/Região como assunto: Europa Idioma: En Ano de publicação: 2019 Tipo de documento: Article
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Impressão Genômica / Transtornos Cromossômicos Tipo de estudo: Diagnostic_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Aged80 / Child / Child, preschool / Humans / Infant / Middle aged / Newborn País/Região como assunto: Europa Idioma: En Ano de publicação: 2019 Tipo de documento: Article