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whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31». Nat Genet (en inglés) 34…

Instituto de Tecnología de Rochester. Panara, Robert F. (1997). On His Deafness and Other Melodies Unheard. Rochester, New York: Deaf Life Press. ISBN 978-0-9634016-5-6…

MJ (2001). «Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure.». Nat. Genet. 29 (3): 310-4. PMID 11687798. S2CID 5892001…

PM, Kenyon JB, Hoover D (Jun 2000). «Tietz syndrome (hypopigmentation/deafness) caused by mutation of MITF» (Free full text). J. Med. Genet. 37 (6): 446-448…

hipoacusia (Partial Deafness Treatment - PDT) usando un método inventado por él - PDCI - implantación coclear en hipoacusia (partial deafness cochlear implantation)…

Cattanach, B (1999). «The 'dalmatian dilemma': white coat colour and deafness». Journal of Small Animal Practice 40 (4): 193-4, 196, 198-200. PMID 10340252…

El síndrome KID (del inglés Keratitis–Ichthyosis–Deafness) o síndrome de queratitis ictiosis sordera, es una enfermedad muy rara de origen congénito que…

intestinales (Cell migration disorder of the neurocytes of the gut) y sordera (Deafness)», según varios portales médicos.[1]​[2]​[3]​ El oftalmólogo neerlandés…

hypertelorism, Pulmonary stenosis, Abnormal genitalia, Retarded growth, Deafness).[1]​[2]​ A este síndrome actualmente se le ha dejado de denominar como…

interna mitocondrial. [Suministrado por OMIM][2]​ «The human family of Deafness/Dystonia peptide (DDP) related mitochondrial import proteins». Genomics…

Unacknowledged detection of auditory stimuli in a patient with cerebral deafness. Cortex 36(1), 71-80 "eye, human."Encyclopædia Britannica from Encyclopædia…

ellos Una introducción a la cultura visual (Paidós, 2003), Silent Poetry. Deafness, sign language and visual culture in Modern France (1995), The Visual Culture…

https://rarediseases.org/gard-rare-disease/knuckle-pads-leuconychia-and-sensorineural-deafness/ RESERVADOS, INSERM US14-- TODOS LOS DERECHOS. «Orphanet: Bart Pumphrey…

with pigmentary anomalies of the iris and head hair and with congenital deafness; Dystopia canthi medialis et punctorum lacrimalium lateroversa, hyperplasia…

febrero de 2018). «Review: ‘This Close,’ a Serious Comedy About Life and Deafness».  «Best TV Shows of 2018 So Far». Vulture. July 2018.  «This Close Is…

2004. Print. Stefanatos GA, Gershkoff A, Madigan S (2005). "On pure word deafness, temporal processing, and the left hemisphere". Journal of the International…

Biologists (1 de noviembre de 2011). «Mouse genetics for studying mechanisms of deafness and more: an interview with Karen Steel». Disease Models & Mechanisms (en…

de noviembre de 2012.  Loui, P.; Alsop, D.; Schlaug, S.; (2009). «Tone Deafness: A New Disconnection Syndrome?». Journal of Neuroscience 29 (33): 10215-10220…

«Entrez Gene: TMC2 transmembrane channel-like 2».  «Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell…

California, Northridge, Deaf West Theatre, Greater Los Angeles Agency on Deafness (GLAD), la Fundación Greenelight, y el Departamento de Policía de Los Ángeles…