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Spectrum of Genetic Diseases in Tunisia: Current Situation and Main Milestones Achieved.
Mezzi, Nessrine; Messaoud, Olfa; Mkaouar, Rahma; Zitouna, Nadia; Romdhane, Safa; Abdessalem, Ghaith; Charfeddine, Cherine; Maazoul, Faouzi; Ouerteni, Ines; Hamdi, Yosr; Zaouak, Anissa; Mrad, Ridha; Abdelhak, Sonia; Romdhane, Lilia.
Afiliación
  • Mezzi N; Laboratory of Biomedical Genomics and Oncogenetics, Institut Pasteur de Tunis, Tunis 1002, Tunisia.
  • Messaoud O; Department of Biology, Faculty of Sciences of Bizerte, Université Tunis Carthage, Jarzouna 7021, Tunisia.
  • Mkaouar R; Laboratory of Biomedical Genomics and Oncogenetics, Institut Pasteur de Tunis, Tunis 1002, Tunisia.
  • Zitouna N; Laboratory of Biomedical Genomics and Oncogenetics, Institut Pasteur de Tunis, Tunis 1002, Tunisia.
  • Romdhane S; Laboratory of Biomedical Genomics and Oncogenetics, Institut Pasteur de Tunis, Tunis 1002, Tunisia.
  • Abdessalem G; Laboratory of Biomedical Genomics and Oncogenetics, Institut Pasteur de Tunis, Tunis 1002, Tunisia.
  • Charfeddine C; Laboratory of Biomedical Genomics and Oncogenetics, Institut Pasteur de Tunis, Tunis 1002, Tunisia.
  • Maazoul F; Laboratory of Biomedical Genomics and Oncogenetics, Institut Pasteur de Tunis, Tunis 1002, Tunisia.
  • Ouerteni I; High Institute of Biotechnology of Sidi Thabet, Biotechpole of Sidi Thabet, University of Manouba, Ariana 2080, Tunisia.
  • Hamdi Y; Department of Congenital and Hereditary Diseases, Charles Nicolle Hospital, Tunis 1002, Tunisia.
  • Zaouak A; Department of Congenital and Hereditary Diseases, Charles Nicolle Hospital, Tunis 1002, Tunisia.
  • Mrad R; Laboratory of Biomedical Genomics and Oncogenetics, Institut Pasteur de Tunis, Tunis 1002, Tunisia.
  • Abdelhak S; Laboratory of Human and Experimental Pathology, Institut Pasteur de Tunis, Tunis 1002, Tunisia.
  • Romdhane L; Department of Dermatology, Research Unit Genodermatosis and Cancer LR12SP03, Habib Thameur Hospital, Faculty of Medicine of Tunis, University of Tunis El Manar, Tunis 1002, Tunisia.
Genes (Basel) ; 12(11)2021 11 19.
Article en En | MEDLINE | ID: mdl-34828426
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Población / Enfermedades Genéticas Congénitas Tipo de estudio: Risk_factors_studies / Screening_studies / Systematic_reviews Límite: Humans País/Región como asunto: Africa Idioma: En Revista: Genes (Basel) Año: 2021 Tipo del documento: Article País de afiliación: Túnez
Texto completo
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Población / Enfermedades Genéticas Congénitas Tipo de estudio: Risk_factors_studies / Screening_studies / Systematic_reviews Límite: Humans País/Región como asunto: Africa Idioma: En Revista: Genes (Basel) Año: 2021 Tipo del documento: Article País de afiliación: Túnez