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Haplotype analysis of the X chromosome in patients with Turner syndrome in order to verify the possible effect of imprinting on selected symptoms.
Vrtel, Petr; Vrtel, Radek; Klaskova, Eva; Vrbicka, Dita; Adamova, Katerina; Pavlicek, Jan; Hana, Vaclav; Hana, Vaclav; Soucek, Ondrej; Stara, Veronika; Lebl, Jan; Snajdrova, Marta; Zapletalova, Jirina; Furst, Tomas; Kapralova, Sabina; Tauber, Zdenek; Krejcirikova, Eva; Routilova, Marketa; Stellmachova, Julia; Vodicka, Radek; Prochazka, Martin.
Afiliação
  • Vrtel P; Department of Medical Genetics, Faculty of Medicine and Dentistry, Palacky University Olomouc and University Hospital Olomouc, Czech Republic.
  • Vrtel R; Department of Medical Genetics, Faculty of Medicine and Dentistry, Palacky University Olomouc and University Hospital Olomouc, Czech Republic.
  • Klaskova E; Department of Paediatrics, Faculty of Medicine and Dentistry, Palacky University Olomouc and University Hospital Olomouc, Czech Republic.
  • Vrbicka D; Department of Medical Genetics, Faculty of Medicine and Dentistry, Palacky University Olomouc and University Hospital Olomouc, Czech Republic.
  • Adamova K; Department of Medical Genetics, Faculty of Medicine and Dentistry, Palacky University Olomouc and University Hospital Olomouc, Czech Republic.
  • Pavlicek J; Department of Paediatrics and Neonatal Care, Faculty of Medicine, University of Ostrava, Ostrava, Czech Republic.
  • Hana V; 3rd Department of Medicine - Department of Endocrinology and Metabolism, 1st Faculty of Medicine, Charles University in Prague, Czech Republic.
  • Hana V; 3rd Department of Medicine - Department of Endocrinology and Metabolism, 1st Faculty of Medicine, Charles University in Prague, Czech Republic.
  • Soucek O; Department of Paediatrics, Motol University Hospital, Prague, Czech Republic.
  • Stara V; Department of Paediatrics, 2nd Faculty of Medicine, Charles University in Prague, Czech Republic.
  • Lebl J; Department of Paediatrics, 2nd Faculty of Medicine, Charles University in Prague, Czech Republic.
  • Snajdrova M; Department of Paediatrics, Motol University Hospital, Prague, Czech Republic.
  • Zapletalova J; Department of Paediatrics, Faculty of Medicine and Dentistry, Palacky University Olomouc and University Hospital Olomouc, Czech Republic.
  • Furst T; Department of Mathematical Analysis and Applications of Mathematics, Faculty of Science, Palacky University Olomouc, Czech Republic.
  • Kapralova S; Department of Paediatrics, Faculty of Medicine and Dentistry, Palacky University Olomouc and University Hospital Olomouc, Czech Republic.
  • Tauber Z; Department of Histology and Embryology, Palacky University Olomouc and University Hospital Olomouc, Czech Republic.
  • Krejcirikova E; Department of Medical Genetics, Faculty of Medicine and Dentistry, Palacky University Olomouc and University Hospital Olomouc, Czech Republic.
  • Routilova M; Department of Medical Genetics, Faculty of Medicine and Dentistry, Palacky University Olomouc and University Hospital Olomouc, Czech Republic.
  • Stellmachova J; Department of Medical Genetics, Faculty of Medicine and Dentistry, Palacky University Olomouc and University Hospital Olomouc, Czech Republic.
  • Vodicka R; Department of Medical Genetics, Faculty of Medicine and Dentistry, Palacky University Olomouc and University Hospital Olomouc, Czech Republic.
  • Prochazka M; Department of Medical Genetics, Faculty of Medicine and Dentistry, Palacky University Olomouc and University Hospital Olomouc, Czech Republic.
Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub ; 166(1): 63-67, 2022 Mar.
Article em En | MEDLINE | ID: mdl-33463629
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Turner / Cardiopatias Congênitas Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Turner / Cardiopatias Congênitas Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article