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Apparent Homozygosity of p.Phe508del in CFTR due to a Large Gene Deletion of Exons 4-11.
Neocleous, Vassos; Yiallouros, Panayiotis K; Tanteles, George A; Costi, Constantina; Moutafi, Maria; Ioannou, Phivos; Patsalis, Philippos C; Sismani, Carolina; Phylactou, Leonidas A.
Afiliação
  • Neocleous V; Department of Molecular Genetics, Function and Therapy, The Cyprus Institute of Neurology and Genetics, P.O. Box 23462, 1683 Nicosia, Cyprus.
  • Yiallouros PK; Department of Pediatrics, Hospital "Archbishop Makarios III", 1474 Nicosia, Cyprus ; Cyprus International Institute for Environmental & Public Health in Association with Harvard School of Public Health, Cyprus University of Technology, 95 Irenes Street, 3041 Limassol, Cyprus.
  • Tanteles GA; Department of Clinical Genetics, The Cyprus Institute of Neurology and Genetics, P.O. Box 23462, 1683 Nicosia, Cyprus.
  • Costi C; Department of Molecular Genetics, Function and Therapy, The Cyprus Institute of Neurology and Genetics, P.O. Box 23462, 1683 Nicosia, Cyprus.
  • Moutafi M; Department of Cytogenetics and Genomics, The Cyprus Institute of Neurology and Genetics, P.O. Box 23462, 1683 Nicosia, Cyprus.
  • Ioannou P; Department of Pediatrics, Hospital "Archbishop Makarios III", 1474 Nicosia, Cyprus.
  • Patsalis PC; Translational Genomics Team, The Cyprus Institute of Neurology and Genetics, P.O. Box 23462, 1683 Nicosia, Cyprus.
  • Sismani C; Department of Cytogenetics and Genomics, The Cyprus Institute of Neurology and Genetics, P.O. Box 23462, 1683 Nicosia, Cyprus.
  • Phylactou LA; Department of Molecular Genetics, Function and Therapy, The Cyprus Institute of Neurology and Genetics, P.O. Box 23462, 1683 Nicosia, Cyprus.
Case Rep Genet ; 2014: 613863, 2014.
Article em En | MEDLINE | ID: mdl-24649380
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Case Rep Genet Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Chipre
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Case Rep Genet Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Chipre