Related Experiment Videos
The history of the genetics of hearing impairment
1Department of Otolaryngology, Albert Einstein College of Medicine of Yeshiva University, Bronx, New York.
Annals of the New York Academy of Sciences
|January 1, 1991
Abstract
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
A time frame of critical/sensitive periods of language development.
Indian journal of otolaryngology and head and neck surgery : official publication of the Association of Otolaryngologists of India·2012
Neurophysiological indices of language impairment in children.
Acta oto-laryngologica·2001
Efficacy of ofloxacin and other otic preparations for otitis externa.
The Pediatric infectious disease journal·2001
Redefining the survival of the fittest: communication disorders in the 21st century.
The Laryngoscope·2000
Reversible sensorineural hearing loss following administration of muromonab-CD3 (OKT3) for cadaveric renal transplant immunosuppression.
The Annals of otology, rhinology, and laryngology·2000
Structure of Musical Dislikes: Findings From Multiple Genres and Countries.
Annals of the New York Academy of Sciences·2026
A DRACH Observed/Expected Metric Reveals the Evolutionary Landscape of Epitranscriptomic Regulation Across Bilateria.
Annals of the New York Academy of Sciences·2026
Evolutionary Background of Precise Vocal-Respiratory Temporal Coordination in Human Infants.
Annals of the New York Academy of Sciences·2026
Tropical Easterly Waves in the Tropical North Atlantic Basin.
Annals of the New York Academy of Sciences·2026
Dynamic Adaptation Responses to Auditory Perturbations During Walking in Multiple Sclerosis With Progressive Subtypes.
Annals of the New York Academy of Sciences·2026
Initial Evidence of Mathematics Interpretation Bias Intervention Effects on College Students' Mathematics Anxiety.
Annals of the New York Academy of Sciences·2026
Caregiver's perspectives toward genome sequencing in children with neurodevelopmental disorders: Integrating genomic information into pediatric care.
Current problems in pediatric and adolescent health care·2026
Father and son with a pathogenic variant c.614dup p.(Gln206Thrfs*20) in the NR5A1 gene: a case report.
Frontiers in pediatrics·2026
Pediatric Spinal Cord Astrocytoma With Granular Cell-Like Morphology and KIAA1549::BRAF Fusion.
Neuropathology : official journal of the Japanese Society of Neuropathology·2026
KCTD1 p.Gly62Asp Variant in Scalp-Ear-Nipple Syndrome: Phenotypic and Structural Insights.
The Journal of craniofacial surgery·2026
Schizophrenia-associated polygenic liability and structural genomic risk demonstrate broadly distributed neuropsychiatric associations in the All of Us Research Program.
medRxiv : the preprint server for health sciences·2026