Last Posted: Dec-23-2016 2PM
From CDC Information Database
This database includes general CDC public health information on specific diseases and health related topics. When available, the database displays genomic information from various CDC web pages. Users are also encouraged to conduct searches of CDC website for additional information.
- Beyond the Blood Spot: Newborn Screening for Hearing Loss and Critical Congenital Heart Disease
CDC Public Health Grand Rounds, Septemeber 20, 2016 - Protect Your Hearing, Promote Hearing Health
- CDC Information: Doctors and Infant Hearing
How Children Can Be "Lost" to the Early Hearing System - CDC Information: About 1 out of 2 cases of hearing loss in babies is due to genetic causes
- CDC Information: Amy?s Story- All in the Family
- CDC Information: Amy?s Story- All in the Family
From Implementation Database
This database focuses on state and national activities that integrate genomics into public health programs and clinical practice
- Newborn Screening Home
[Disease: NA; Type: Program; State: Indiana] - Center for Congenital and Inherited Disorders (CCID)
[Disease: Birth defects; Type: General Info; State: Iowa] - Newborn Screening Program (Minnesota)
[Disease: NA; Type: Program; State: Minnesota] - Genetic Disease & Early Childhood
[Disease: Birth defects; Type: Program; State: Missouri] - Newborn Screening Tests (New Jersey)
[Disease: NA; Type: Program; State: New Jersey]
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.
- 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)
From HuGE Literature Finder Database
This database contains published literature on genetic associations and other human genome epidemiology
- A common variant in CLDN14 causes precipitous, prelingual sensorineural hearing loss in multiple families due to founder effect.
Human genetics 2016 Nov .
Pater Justin A, Benteau Tammy, Griffin Anne, Penney Cindy, Stanton Susan G, Predham Sarah, Kielley Bernadine, Squires Jessica, Zhou Jiayi, Li Quan, Abdelfatah Nelly, O'Rielly Darren D, Young Terry-Ly - The role of alternative GJB2 transcription in screening for neonatal sensorineural deafness in Austria.
Acta oto-laryngologica 2016 Nov 1-5.
Parzefall Thomas, Lucas Trevor, Koenighofer Martin, Ramsebner Reinhard, Frohne Alexandra, Czeiger Shelly, Baumgartner Wolf-Dieter, Schoefer Christian, Gstoettner Wolfgang, Frei Kleme - A genotypic ascertainment approach to refute the association of MYO1A variants with non-syndromic deafness.
European journal of human genetics : EJHG 2016 Oct .
Patton John, Brewer Carmen, Chien Wade, Johnston Jennifer J, Griffith Andrew J, Biesecker Leslie - Deafness genes in families with non-syndromic hearing loss in Shandong, China: a genetic study.
Lancet (London, England) 2016 Oct 388 Suppl 1 S80.
Bai Xiaohui, Xu Lei, Zhang Fengguo, Xiao Yun, Li Jianfeng, Wang Hai - Pitch and Loudness Tinnitus in Individuals with Presbycusis.
International archives of otorhinolaryngology 2016 Oct 20 (4): 321-326.
Seimetz Bruna Macangnin, Teixeira Adriane Ribeiro, Rosito Leticia Petersen Schmidt, Flores Leticia Sousa, Pappen Carlos Henrique, Dall'igna Cel
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