hearing loss phenotype

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Mentioned in (27)

Papers in which this entity is mentioned.

• Nkx2.7 is a conserved regulator of craniofacial development. (2025)
• A global multicohort study to map subcortical brain development and cognition in infancy and early childhood. (2024)
• Delayed cortical thinning in children and adolescents with prenatal alcohol exposure. (2023)
• Early neurodevelopment of HIV-exposed uninfected children in the era of antiretroviral therapy: a systematic review and meta-analysis. (2022)
• Best practices for variant calling in clinical sequencing. (2020)
• Neurodevelopment of HIV-exposed uninfected children in South Africa: outcomes from an observational birth cohort study. (2019)
• Risk for Speech and Language Impairments in Preschool Age HIV-exposed Uninfected Children With In Utero Combination Antiretroviral Exposure. (2018)
• Prevalence of Autism Spectrum Disorder Among Children Aged 8 Years - Autism and Developmental Disabilities Monitoring Network, 11 Sites, United States, 2014. (2018)
• Alcohol's Effects on the Brain: Neuroimaging Results in Humans and Animal Models. (2017)
• Epidemiology, Etiology, and Treatment of Isolated Cleft Palate. (2016)
• A review of the nonpressor and nonantidiuretic actions of the hormone vasopressin. (2015)
• Early steps in inner ear development: induction and morphogenesis of the otic placode. (2015)
• The sox family of transcription factors: versatile regulators of stem and progenitor cell fate. (2013)
• Developmental outcome of very low birth weight infants in a developing country. (2012)
• Auditory brainstem response (ABR) abnormalities across the life span of rats prenatally exposed to alcohol. (2012)
• Delays in auditory processing identified in preschool children with FASD. (2012)
• Molecular and phenotypic aspects of CHD7 mutation in CHARGE syndrome. (2010)
• Novelty P3 reductions in depression: characterization using principal components analysis (PCA) of current source density (CSD) waveforms. (2010)
• FGF signaling regulates otic placode induction and refinement by controlling both ectodermal target genes and hindbrain Wnt8a. (2010)
• A genome-wide association study of autism reveals a common novel risk locus at 5p14.1. (2009)
• Novel SOX2 mutations and genotype-phenotype correlation in anophthalmia and microphthalmia. (2009)
• A neural crest deficit in Down syndrome mice is associated with deficient mitotic response to Sonic hedgehog. (2009)
• Neurotoxic effects and biomarkers of lead exposure: a review. (2009)
• A neural network critical for spelling. (2009)
• Otitis media in a mouse model for Down syndrome. (2009)
• Mutations within Sox2/SOX2 are associated with abnormalities in the hypothalamo-pituitary-gonadal axis in mice and humans. (2006)
• Decline of the critical period of visual plasticity is concurrent with the reduction of NR2B subunit of the synaptic NMDA receptor in layer 4. (2003)

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