Etiology of unilateral hearing loss in a national hereditary deafness repository.

[1]  A. Pandya,et al.  Impact of co-occurring birth defects on the timing of newborn hearing screening and diagnosis. , 2011, American journal of audiology.

[2]  Sun O Chang,et al.  Unilateral Sensorineural Hearing Loss in Children: The Importance of Temporal Bone Computed Tomography and Audiometric Follow-Up , 2009, Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology.

[3]  W. Nance,et al.  Familial unilateral deafness and delayed endolymphatic hydrops , 2007, American journal of medical genetics. Part A.

[4]  S. Boppana,et al.  GJB2 and GJB6 Mutations in Children with Congenital Cytomegalovirus Infection , 2007, Pediatric Research.

[5]  S. Rosengren,et al.  Transcriptional control of SLC26A4 is involved in Pendred syndrome and nonsyndromic enlargement of vestibular aqueduct (DFNB4). , 2007, American journal of human genetics.

[6]  C. Morton,et al.  Newborn hearing screening--a silent revolution. , 2006, The New England journal of medicine.

[7]  J. Lieu,et al.  Speech-language and educational consequences of unilateral hearing loss in children. , 2004, Archives of otolaryngology--head & neck surgery.

[8]  J. Weigelt,et al.  NMR structure of the LCCL domain and implications for DFNA9 deafness disorder , 2001, The EMBO journal.

[9]  Michael P. Gorga,et al.  Identification of Neonatal Hearing Impairment: Hearing Status at 8 to 12 Months Corrected Age Using a Visual Reinforcement Audiometry Protocol , 2000, Ear and hearing.

[10]  J. Beckmann,et al.  An alpha-tectorin gene defect causes a newly identified autosomal recessive form of sensorineural pre-lingual non-syndromic deafness, DFNB21. , 1999, Human molecular genetics.

[11]  T. Finitzo,et al.  The newborn with hearing loss: detection in the nursery. , 1998, Pediatrics.

[12]  Christine E. Seidman,et al.  Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction , 1998, Nature Genetics.

[13]  D. Brody,et al.  Prevalence of hearing loss among children 6 to 19 years of age: the Third National Health and Nutrition Examination Survey. , 1998, JAMA.

[14]  V. Thomson,et al.  Newborn Hearing Screening: The Great Omission , 1998, Pediatrics.

[15]  L. Barsky-Firkser,et al.  Universal newborn hearing screenings: a three-year experience. , 1997, Pediatrics.

[16]  A. Pandya,et al.  Mutation in the mitochondrial 12S rRNA gene in two families from Mongolia with matrilineal aminoglycoside ototoxicity. , 1997, Journal of medical genetics.

[17]  K. Arnos,et al.  Genetic epidemiological studies of early-onset deafness in the U.S. school-age population. , 1993, American journal of medical genetics.

[18]  W. J. Kelly,et al.  Unilateral hearing loss in children , 1991, The Laryngoscope.

[19]  W. Rutter,et al.  Polymorphic DNA region adjacent to the 5' end of the human insulin gene. , 1981, Proceedings of the National Academy of Sciences of the United States of America.

[20]  G. Everberg LIII Etiology of Unilateral Total Deafness Studied in a Series of Children and Young Adults , 1960 .

[21]  K. Steel,et al.  Mutations in connexin31 underlie recessive as well as dominant non-syndromic hearing loss. , 2000, Human molecular genetics.

[22]  G. Richardson,et al.  Mutations in the human α-tectorin gene cause autosomal dominant non-syndromic hearing impairment , 1998, Nature Genetics.

[23]  G. Everberg Further studies on hereditary unilateral deafness. , 1960, Acta oto-laryngologica.