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Application of Chromosome Microarray Analysis in the Investigation of Developmental Disabilities and Congenital Anomalies: Single Center Experience and Review of NRXN3 and NEDD4L Deletions.
Çebi, Alper Han; Altiner, Sule.
Afiliación
  • Çebi AH; Department of Medical Genetics, Karadeniz Technical University School of Medicine, Trabzon, Turkey.
  • Altiner S; Department of Medical Genetics, University of Health Sciences, Trabzon Kanuni Training and Research Hospital, Trabzon, Turkey.
Mol Syndromol ; 11(4): 197-206, 2020 Nov.
Article en En | MEDLINE | ID: mdl-33224013

Texto completo: 1 Bases de datos: MEDLINE Tipo de estudio: Observational_studies / Risk_factors_studies Idioma: En Revista: Mol Syndromol Año: 2020 Tipo del documento: Article País de afiliación: Turquía

Texto completo: 1 Bases de datos: MEDLINE Tipo de estudio: Observational_studies / Risk_factors_studies Idioma: En Revista: Mol Syndromol Año: 2020 Tipo del documento: Article País de afiliación: Turquía