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Complex translocation leading to13q interstitial deletion in a Moroccan child with retinoblastoma and intellectual disability.
El Amrani, Zhour; Elalaoui, Siham Chafai; Jdioui, Wafae; Sbiti, Aziza; Ratbi, Ilham; Liehr, Thomas; Sefiani, Abdelaziz; Natiq, Abdelhafid.
Afiliação
  • El Amrani Z; RABAT Research team in genomics and molecular epidemiology of genetic diseases, Genomics Center of Human Pathologies, Faculty of Medicine and Pharmacy, University Mohammed V, Rabat, Morocco.
  • Elalaoui SC; Département de Génétique Médicale, Institut National d'Hygiène, Rabat, Morocco.
  • Jdioui W; RABAT Research team in genomics and molecular epidemiology of genetic diseases, Genomics Center of Human Pathologies, Faculty of Medicine and Pharmacy, University Mohammed V, Rabat, Morocco.
  • Sbiti A; Département de Génétique Médicale, Institut National d'Hygiène, Rabat, Morocco.
  • Ratbi I; médicale, Centre des consultations et des explorations externes, Hopital d'enfants, CHU Ibn SinaConsultation de génétique, Rabat, Marocco.
  • Liehr T; RABAT Research team in genomics and molecular epidemiology of genetic diseases, Genomics Center of Human Pathologies, Faculty of Medicine and Pharmacy, University Mohammed V, Rabat, Morocco.
  • Sefiani A; Département de Génétique Médicale, Institut National d'Hygiène, Rabat, Morocco.
  • Natiq A; RABAT Research team in genomics and molecular epidemiology of genetic diseases, Genomics Center of Human Pathologies, Faculty of Medicine and Pharmacy, University Mohammed V, Rabat, Morocco.
Ophthalmic Genet ; 43(5): 689-692, 2022 10.
Article em En | MEDLINE | ID: mdl-35658784
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Retinoblastoma / Neoplasias da Retina / Deficiência Intelectual Limite: Humans Idioma: En Revista: Ophthalmic Genet Assunto da revista: GENETICA MEDICA / OFTALMOLOGIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Marrocos
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Retinoblastoma / Neoplasias da Retina / Deficiência Intelectual Limite: Humans Idioma: En Revista: Ophthalmic Genet Assunto da revista: GENETICA MEDICA / OFTALMOLOGIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Marrocos