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Correction: Broadening the phenotypic spectrum of pathogenic LARP7 variants: two cases with intellectual disability, variable growth retardation and distinct facial features.
Hollink, Iris H I M; Alfadhel, Majid; Al-Wakeel, Anwar S; Ababneh, Farough; Pfundt, Rolph; de Man, Stella A; Abou Jamra, Rami; Rolfs, Arndt; Bertoli-Avella, Aida M; van de Laar, Ingrid M B H.
Afiliación
  • Hollink IHIM; Department of Clinical Genetics, Erasmus Medical Center, Rotterdam, The Netherlands.
  • Alfadhel M; Division of Genetics, Department of Pediatrics, King Saud bin Abdulaziz University for Health Sciences, King Abdullah Specialized Children's Hospital, King Abdulaziz Mecial City, Riyadh, Saudi Arabia.
  • Al-Wakeel AS; Division of Genetics, Department of Pediatrics, King Saud bin Abdulaziz University for Health Sciences, King Abdullah Specialized Children's Hospital, King Abdulaziz Mecial City, Riyadh, Saudi Arabia.
  • Ababneh F; Division of Genetics, Department of Pediatrics, King Saud bin Abdulaziz University for Health Sciences, King Abdullah Specialized Children's Hospital, King Abdulaziz Mecial City, Riyadh, Saudi Arabia.
  • Pfundt R; Department of Human Genetics, Division of Genome Diagnostics, Radboud University Medical Centre, Nijmegen, The Netherlands.
  • de Man SA; Department of Clinical Genetics, Erasmus Medical Center, Rotterdam, The Netherlands.
  • Abou Jamra R; Department of Pediatrics, Amphia Hospital, Breda, The Netherlands.
  • Rolfs A; Centogene AG, Rostock, Germany.
  • Bertoli-Avella AM; Centogene AG, Rostock, Germany.
  • van de Laar IMBH; Albrecht-Kossel-Institute for Neuroregeneration, Medical University Rostock, Rostock, Germany.
J Hum Genet ; 63(4): 539, 2018 04.
Article en En | MEDLINE | ID: mdl-29576627

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: J Hum Genet Asunto de la revista: GENETICA MEDICA Año: 2018 Tipo del documento: Article País de afiliación: Países Bajos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: J Hum Genet Asunto de la revista: GENETICA MEDICA Año: 2018 Tipo del documento: Article País de afiliación: Países Bajos