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X-linked recessive ichthyosis in 8 Tunisian patients: awareness of misdiagnosis due to the technical trap of the STS pseudogene.
Chouk, Hamza; Saad, Sarra; Dimassi, Sarra; Fetoui, Nadia Ghariani; Bennour, Ayda; Gammoudi, Rima; Elmabrouk, Haifa; Saad, Ali; Denguezli, Mohamed; H'mida, Dorra.
Afiliação
  • Chouk H; Department of Cytogenetics, Molecular Genetic and Biology of Human Reproduction, Farhat Hached of Sousse, Sousse, Tunisia.
  • Saad S; Higher Institute of Biotechnology of Monastir, Monastir, Tunisia.
  • Dimassi S; Faculty of Medicine of Sousse, Sousse, Tunisia.
  • Fetoui NG; Department of Dermatology, Farhat Hached, Sousse, Tunisia.
  • Bennour A; Department of Cytogenetics, Molecular Genetic and Biology of Human Reproduction, Farhat Hached of Sousse, Sousse, Tunisia.
  • Gammoudi R; Faculty of Medicine of Sousse, Sousse, Tunisia.
  • Elmabrouk H; Faculty of Medicine of Sousse, Sousse, Tunisia.
  • Saad A; Department of Dermatology, Farhat Hached, Sousse, Tunisia.
  • Denguezli M; Department of Cytogenetics, Molecular Genetic and Biology of Human Reproduction, Farhat Hached of Sousse, Sousse, Tunisia.
  • H'mida D; Faculty of Medicine of Sousse, Sousse, Tunisia.
BMC Med Genomics ; 15(1): 165, 2022 07 26.
Article em En | MEDLINE | ID: mdl-35883075
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pseudogenes / Ictiose Ligada ao Cromossomo X 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: Pseudogenes / Ictiose Ligada ao Cromossomo X Idioma: En Ano de publicação: 2022 Tipo de documento: Article