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Non lethal Raine syndrome and differential diagnosis.
Elalaoui, Siham Chafai; Al-Sheqaih, Nada; Ratbi, Ilham; Urquhart, Jill E; O'Sullivan, James; Bhaskar, Sanjeev; Williams, Simon S; Elalloussi, Mustapha; Lyahyai, Jaber; Sbihi, Leila; Cherkaoui Jaouad, Imane; Sbihi, Abdelhafid; Newman, William G; Sefiani, Abdelaziz.
Affiliation
  • Elalaoui SC; Centre de Génomique Humaine, Faculté de Médecine et de Pharmacie, Université Mohammed V Souissi, Rabat, Morocco; Département de Génétique Médicale, Institut National d'Hygiène, Rabat, Morocco. Electronic address: sihamgen@yahoo.fr.
  • Al-Sheqaih N; Manchester Centre for Genomic Medicine, St. Mary's Hospital, Manchester Academic Health Sciences Centre, Manchester, M13 9WL, UK; Manchester Centre for Genomic Medicine, Institute of Human Development, University of Manchester, Manchester, M13 9WL, UK.
  • Ratbi I; Centre de Génomique Humaine, Faculté de Médecine et de Pharmacie, Université Mohammed V Souissi, Rabat, Morocco.
  • Urquhart JE; Manchester Centre for Genomic Medicine, St. Mary's Hospital, Manchester Academic Health Sciences Centre, Manchester, M13 9WL, UK; Manchester Centre for Genomic Medicine, Institute of Human Development, University of Manchester, Manchester, M13 9WL, UK.
  • O'Sullivan J; Manchester Centre for Genomic Medicine, St. Mary's Hospital, Manchester Academic Health Sciences Centre, Manchester, M13 9WL, UK; Manchester Centre for Genomic Medicine, Institute of Human Development, University of Manchester, Manchester, M13 9WL, UK.
  • Bhaskar S; Manchester Centre for Genomic Medicine, St. Mary's Hospital, Manchester Academic Health Sciences Centre, Manchester, M13 9WL, UK.
  • Williams SS; Manchester Centre for Genomic Medicine, St. Mary's Hospital, Manchester Academic Health Sciences Centre, Manchester, M13 9WL, UK.
  • Elalloussi M; Service d'Odontologie Pédiatrique, Faculté de Médecine Dentaire, Université Mohammed V, Rabat, Morocco.
  • Lyahyai J; Centre de Génomique Humaine, Faculté de Médecine et de Pharmacie, Université Mohammed V Souissi, Rabat, Morocco.
  • Sbihi L; Service de Radiologie, Hopital Ibn Sina, Rabat, Morocco.
  • Cherkaoui Jaouad I; Centre de Génomique Humaine, Faculté de Médecine et de Pharmacie, Université Mohammed V Souissi, Rabat, Morocco; Département de Génétique Médicale, Institut National d'Hygiène, Rabat, Morocco.
  • Sbihi A; Cabinet de Radiologie de l'Agdal, Rabat, Morocco.
  • Newman WG; Manchester Centre for Genomic Medicine, St. Mary's Hospital, Manchester Academic Health Sciences Centre, Manchester, M13 9WL, UK; Manchester Centre for Genomic Medicine, Institute of Human Development, University of Manchester, Manchester, M13 9WL, UK.
  • Sefiani A; Centre de Génomique Humaine, Faculté de Médecine et de Pharmacie, Université Mohammed V Souissi, Rabat, Morocco; Département de Génétique Médicale, Institut National d'Hygiène, Rabat, Morocco.
Eur J Med Genet ; 59(11): 577-583, 2016 Nov.
Article in En | MEDLINE | ID: mdl-27667191
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Osteosclerosis / Abnormalities, Multiple / Exophthalmos / Extracellular Matrix Proteins / Cleft Palate / Dementia / Casein Kinase I / Diagnosis, Differential / Epilepsy / Amelogenesis Imperfecta Type of study: Diagnostic_studies / Prognostic_studies Language: En Journal: Eur J Med Genet Journal subject: GENETICA MEDICA Year: 2016 Document type: Article
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Osteosclerosis / Abnormalities, Multiple / Exophthalmos / Extracellular Matrix Proteins / Cleft Palate / Dementia / Casein Kinase I / Diagnosis, Differential / Epilepsy / Amelogenesis Imperfecta Type of study: Diagnostic_studies / Prognostic_studies Language: En Journal: Eur J Med Genet Journal subject: GENETICA MEDICA Year: 2016 Document type: Article