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Last Posted: May 18, 2017

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• Can your baby hear you say “I love you?” 
• Development of a 22q11DS psycho-educational programme: exploration of the views, concerns and educational needs of parents caring for children or adolescents with 22q11DS in relation to mental health issues.  
  Alugo T et al. Child: care, health and development 2017 Mar
• Advances in genetic hearing loss: CIB2 gene.  
  Jacoszek Agnieszka et al. European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery 2016 Oct
• Congenital hearing loss.  
  Korver Anna M H et al. Nature reviews. Disease primers 2017 316094
• Gene therapy: Deaf to hearing a whisper  
  J Gallagher, BBC, February 7, 2017
• Navigating genetic diagnostics in patients with hearing loss.  
  Sloan-Heggen Christina M et al. Current opinion in pediatrics 2016 Dec (6) 705-712
• Too Loud! For Too Long! Loud noises damage hearing 
  CDC Vital Signs, February 2017
• The diagnostic yield of whole-exome sequencing targeting a gene panel for hearing impairment in The Netherlands.  
  Zazo Seco Celia et al. European journal of human genetics : EJHG 2016 Dec
• Application of SNPscan in Genetic Screening for Common Hearing Loss Genes.  
  Gao Zixuan et al. PloS one 2016 11(10) e0165650
• International Pediatric Otolaryngology Group (IPOG) consensus recommendations: Hearing loss in the pediatric patient.  
  Liming Bryan J et al. International journal of pediatric otorhinolaryngology 2016 Nov 90251-258
• Beyond the Blood Spot: Newborn Screening for Hearing Loss and Critical Congenital Heart Disease
  CDC Public Health Grand Rounds, Septemeber 20, 2016
• Concurrent Genetic and Standard Screening for Hearing Impairment in 9317 Southern Chinese Newborns.  
  Peng Qi et al. Genetic testing and molecular biomarkers 2016 Aug
• Outcomes of evaluation and testing of 660 individuals with hearing loss in a pediatric genetics of hearing loss clinic.  
  Mehta Devanshi et al. American journal of medical genetics. Part A 2016 Aug
• Molecular newborn screening of four genetic diseases in Guizhou Province of South China.  
  Huang Shengwen et al. Gene 2016 Jul
• Newborn genetic screening for hearing impairment: a population-based longitudinal study.  
  Wu Chen-Chi et al. Genetics in medicine : official journal of the American College of Medical Genetics 2016 Jun
• New insights in the interpretation of array-CGH: autism spectrum disorder and positive family history for intellectual disability predict the detection of pathogenic variants.  
  Cappuccio Gerarda et al. Italian journal of pediatrics 2016 42(1) 39

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