Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Sarah K. Burton"'
Autor:
Kara A. Withrow, Arti Pandya, Virginia W. Norris, Kelly A. Tracy, Kathleen S. Arnos, Hermine H. Maes, Sarah K. Burton
Publikováno v:
American Journal of Medical Genetics Part A. :1159-1168
Hearing loss is a common neuro-sensory deficit; nearly 50% of children with hearing loss have a genetic etiology. With the discovery of 40 genes and more than 100 loci involved in hearing loss, genetic testing is becoming more widely available. The i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0fe82ba2f05568a8ebec5d2237c5766
https://doi.org/10.1002/ajmg.a.32800
https://doi.org/10.1002/ajmg.a.32800
Publikováno v:
The ASHA Leader. 11:1-33
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e978f46c2478673620a9f1c9b479ad4b
https://doi.org/10.1044/leader.ftr1.11012006.1
https://doi.org/10.1044/leader.ftr1.11012006.1
Autor:
Kathleen S. Arnos, Hermine H. Maes, Arti Pandya, Kara A. Withrow, Virginia W. Norris, Sarah K. Burton, Kelly A. Tracy
Publikováno v:
Journal of genetic counseling. 18(6)
Hearing loss is a common sensory deficit and more than 50% of affected individuals have a genetic etiology. The discovery of 40 genes and more than 100 loci involved in hearing loss has made genetic testing for some of these genes widely available. G
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6492fa56e1d8a8c80c0ebc64aa455193
https://pubmed.ncbi.nlm.nih.gov/19798556
https://pubmed.ncbi.nlm.nih.gov/19798556
Publikováno v:
Journal of genetic counseling. 17(3)
Genetic services for deafness are being increasingly sought due to the introduction of early hearing detection and intervention programs, as well as the rapid progress in the identification of deafness genes. This study aimed to assess the motivation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b2dbb29edc657b0515402e64e1b0fb3
https://pubmed.ncbi.nlm.nih.gov/18247107
https://pubmed.ncbi.nlm.nih.gov/18247107
Publikováno v:
Genetics in medicine : official journal of the American College of Medical Genetics. 8(12)
Purpose: Progress in identifying genes for deafness together with implementation of universal audiologic screening of newborns has provided the opportunity for more widespread use of molecular tests to detect genetic forms of hearing loss. Efforts to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1bdf802f26ada5b3eb9a8ababf4f4a8
https://pubmed.ncbi.nlm.nih.gov/17172941
https://pubmed.ncbi.nlm.nih.gov/17172941
Autor:
Karl R. White, Susan H. Blanton, Sarah K. Burton, Walter E. Nance, Arti Pandya, Kathleen S. Arnos, Brandt Culpepper
Publikováno v:
Genetics in medicine : official journal of the American College of Medical Genetics. 8(8)
Purpose: Permanent hearing loss at birth or in early childhood is common and has many genetic and environmental causes. Advances in the identification and characterization of genetic forms, combined with the early identification of children through t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78d1046fa3cffe91d7910325d740ff80
https://pubmed.ncbi.nlm.nih.gov/16912582
https://pubmed.ncbi.nlm.nih.gov/16912582
Autor:
Sarah K. Burton-Hunter
Publikováno v:
Computers and the Humanities. 10:217-220
DESPITE THE FACT that the majority of sound changes within a given geographical area, within a given span of time, and within a given sound environment have long been considered regular and reduceable to definite patterns of change, and despite the f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8d11dc4750a3b9bac32c7c47078cd770
https://doi.org/10.1007/bf02426314
https://doi.org/10.1007/bf02426314