Last Posted: May 18, 2017
- 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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