Hearing loss || Public Health Genomics Knowledge Base (v1.2)

Public Health Genomics Knowledge Base (v1.2)

From Guideline Database

This database contains updated guidelines, policies and recommendations on genomic research and practice, as provided by professional organizations, federal advisory groups, expert panels and policy groups.

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• Newborn hearing screening programme in Belgium: a consensus recommendation on risk factors.
  Published 2015 (Expert panel)
• Evidence-based guideline summary: Evaluation, diagnosis, and management of facioscapulohumeral muscular dystrophy: Report of the Guideline Development, Dissemination, and Implementation Subcommittee of the American Academy of Neurology and the Practice Issues Review Panel of the American Association of Neuromuscular & Electrodiagnostic Medicine.
  Published 2015 (American Academy of Neurology - Guideline Development, Dissemination, and Implementation Subcommittee) (American Association of Neuromuscular & Electrodiagnostic Medicine - Practice Issues Review Panel)
• American College of Medical Genetics and Genomics guideline for the clinical evaluation and etiologic diagnosis of hearing loss.
  Published 2014 (American College of Medical Genetics and Genomics)

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