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Case Report: Contiguous Xq22.3 Deletion Associated with ATS-ID Syndrome: From Genotype to Further Delineation of the Phenotype.
Smetana, Jan; Vallova, Vladimira; Wayhelova, Marketa; Hladilkova, Eva; Filkova, Hana; Horinova, Vera; Broz, Petr; Mikulasova, Aneta; Gaillyova, Renata; Kuglík, Petr.
Afiliación
  • Smetana J; Department of Genetics and Molecular Biology, Institute of Experimental Biology, Faculty of Science, Masaryk University, Brno, Czech.
  • Vallova V; Department of Genetics and Molecular Biology, Institute of Experimental Biology, Faculty of Science, Masaryk University, Brno, Czech.
  • Wayhelova M; Department of Medical Genetics and Genomics, University Hospital Brno, Brno, Czech.
  • Hladilkova E; Department of Genetics and Molecular Biology, Institute of Experimental Biology, Faculty of Science, Masaryk University, Brno, Czech.
  • Filkova H; Department of Medical Genetics and Genomics, University Hospital Brno, Brno, Czech.
  • Horinova V; Department of Medical Genetics and Genomics, University Hospital Brno, Brno, Czech.
  • Broz P; Department of Medical Genetics and Genomics, University Hospital Brno, Brno, Czech.
  • Mikulasova A; Genetic Ambulance and Counseling, Jihlava, Czech.
  • Gaillyova R; Department of Biology and Medical Genetics, 2nd Faculty of Medicine, Charles University Prague and Faculty Hospital Motol, Prague, Czech.
  • Kuglík P; Biosciences Institute, Newcastle University, Newcastle upon Tyne, United Kingdom.
Front Genet ; 12: 750110, 2021.
Article en En | MEDLINE | ID: mdl-34777475
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Front Genet Año: 2021 Tipo del documento: Article
Texto completo
Añadir a Mi BVS
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PubMed Links
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Front Genet Año: 2021 Tipo del documento: Article