Usher syndrome (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Usher syndrome" in English language version.

refsWebsite

Global rank English rank

28nih.gov

4^th place

20doi.org

2^nd place

9semanticscholar.org

11^th place

8^th place

4web.archive.org

1^st place

2harvard.edu

18^th place

17^th place

1wiley.com

222^nd place

297^th place

1sagepub.com

731^st place

638^th place

1uni-mainz.de

9,571^st place

low place

1worldcat.org

5^th place

1tactiletheworld.wordpress.com

low place

1fuzzywuzzydesign.com

low place

1nalagaat.org.il

low place

doi.org

Otterstedde CR, Spandau U, Blankenagel A, Kimberling WJ, Reisser C (2001). "A new clinical classification for Usher's syndrome based on a new subtype of Usher's syndrome type I". Laryngoscope. 111 (1): 84–86. doi:10.1097/00005537-200101000-00014. PMID 11192904. S2CID 41124463.
Grøndahl J (1987). "Estimation of prognosis and prevalence of retinitis pigmentosa and Usher syndrome in Norway". Clin. Genet. 31 (4): 255–264. doi:10.1111/j.1399-0004.1987.tb02804.x. PMID 3594933. S2CID 26853136.
Pakarinen L, Tuppurainen K, Laipapala P, Mäntyjärvi M, Puhakka H (1996). "The ophthalmological course of Usher syndrome type III". International Ophthalmology. 19 (5): 307–311. doi:10.1007/BF00130927. PMID 8864816. S2CID 26501078.
Keats, Bronya J.B.; Corey, David P. (25 October 2002). "The Usher syndromes". American Journal of Medical Genetics. 89 (3): 158–166. doi:10.1002/(SICI)1096-8628(19990924)89:3<158::AID-AJMG6>3.0.CO;2-#. PMID 10704190. Retrieved 29 June 2022.
Reisser, CFV; Kimberling, WJ; Otterstedde, CR (2002). "Hearing Loss in Usher Syndrome Type II is Nonprogressive". Annals of Otology, Rhinology & Laryngology. 111 (12): 1108–1111. doi:10.1177/000348940211101208. PMID 12498372. S2CID 43346043. Retrieved 4 March 2022.
Sadeghi, Mehdi; Cohn, Edward S.; Kelly, William J.; Kimberling, William J.; Tranebjoerg, Lisbeth; Möller, Claes (2004). "Audiological findings in Usher syndrome types IIa and II (non-IIa)". International Journal of Audiology. 43 (3): 136–143. doi:10.1080/14992020400050019. PMID 15198377. S2CID 40248505.
Hope CI, Bundey S, Proops D, Fielder AR (1997). "Usher syndrome in the city of Birmingham — prevalence and clinical classification". British Journal of Ophthalmology. 81 (1): 46–53. doi:10.1136/bjo.81.1.46. PMC 1721995. PMID 9135408.
Roux AF, Faugere V, Le Guedard S, Pallares-Ruiz N, Vielle A, Chambert S, Marlin S, Hamel C, Gilbert B, Malcolm S, Claustres M (2006). "Survey of the frequency of USH1 gene mutations in a cohort of Usher patients shows the importance of cadherin 23 and protocadherin 15 genes and establishes a detection rate of above 90%". J Med Genet. 43 (9): 763–768. doi:10.1136/jmg.2006.041954. PMC 2564578. PMID 16679490.
Ouyang XM, Yan D, Du LL, Hejtmancik JF, Jacobson SG, Nance WE, Li AR, Angeli S, Kaiser M, Newton V, Brown SD, Balkany T, Liu XZ (2005). "Characterization of Usher syndrome type I gene mutations in an Usher syndrome patient population". Hum Genet. 116 (4): 292–299. doi:10.1007/s00439-004-1227-2. PMID 15660226. S2CID 22812718.
Petit, C (2001). "Usher syndrome: from genetics to pathogenesis" (PDF). Annual Review of Genomics and Human Genetics. 2: 271–97. doi:10.1146/annurev.genom.2.1.271. PMID 11701652. S2CID 505750. Archived from the original (PDF) on 2019-05-03.
Reiners, J; Nagel-Wolfrum, K; Jürgens, K; Märker, T; Wolfrum, U (2006). "Molecular basis of human Usher syndrome: deciphering the meshes of the Usher protein network provides insights into the pathomechanisms of the Usher disease" (PDF). Experimental Eye Research. 83 (1): 97–119. doi:10.1016/j.exer.2005.11.010. PMID 16545802. Archived from the original (PDF) on 2019-05-03.
Gerber, S; Bonneau, D; Gilbert, B; Munnich, A; Dufier, JL; Rozet, JM; Kaplan, J (2006). "USH1A: chronicle of a slow death". American Journal of Human Genetics. 78 (2): 357–9. doi:10.1086/500275. PMC 1380243. PMID 16400615.
Libé-Philippot, Baptiste; Michel, Vincent; Monvel, Jacques Boutet de; Gal, Sébastien Le; Dupont, Typhaine; Avan, Paul; Métin, Christine; Michalski, Nicolas; Petit, Christine (2017-07-25). "Auditory cortex interneuron development requires cadherins operating hair-cell mechanoelectrical transduction". Proceedings of the National Academy of Sciences. 114 (30): 7765–7774. Bibcode:2017PNAS..114.7765L. doi:10.1073/pnas.1703408114. ISSN 0027-8424. PMC 5544301. PMID 28705869.
Smith RJ, Berlin CI, Hejtmancik JF, Keats BJ, Kimberling WJ, Lewis RA, et al. (1994). "Clinical diagnosis of the Usher syndromes. Usher Syndrome Consortium". American Journal of Medical Genetics. 50 (1): 32–38. doi:10.1002/ajmg.1320500107. PMID 8160750.
Fishman GA, Kumar A, Joseph ME, Torok N, Andersonj RJ (1983). "Usher's syndrome: ophthalmic and neuro-otologic findings suggesting genetic heterogeneity". Archives of Ophthalmology. 101 (9): 1367–1374. doi:10.1001/archopht.1983.01040020369005. PMID 6604514.
Williams DS (2007). "Usher syndrome: Animal models, retinal function of Usher proteins, and prospects for gene therapy". Vision Research. 48 (3): 433–41. doi:10.1016/j.visres.2007.08.015. PMC 2680226. PMID 17936325.
Hammerschlag V (1907). "Zur Kenntnis der hereditaer-degenerativen Taubstummen und ihre differential diagnostische Bedeutung". Z. Ohrenheilk. 54: 18–36.
Bell J (1933). Retinitis Pigmentosa and Allied Diseases (2nd ed.). London: Cambridge University Press.
Hallgren B (1959). "Retinitis pigmentosa combined with congenital deafness with vestibulo-cerebellar ataxia and mental abnormality in a proportion of cases: Clinical and geneto-statistical survey". Acta Psychiatr Scand Suppl. 34 (138): 9–101. doi:10.1111/j.1600-0447.1959.tb08605.x. PMID 14399116. S2CID 221393918.
Merin S, Auerbach E (1976). "Retinitis pigmentosa". Surv. Ophthalmol. 20 (5): 303–345. doi:10.1016/S0039-6257(96)90001-6. PMID 817406.
Davenport S, Omenn G (1977). The Heterogeneity of Usher Syndrome (volume 426 ed.). Amsterdam: Excerpta Medica Foundation.
Gorlin R, Tilsner T, Feinstein S, Duvall AJ (1979). "Usher syndrome type III". Arch. Otolaryngol. 105 (6): 353–354. doi:10.1001/archotol.1979.00790180051011. PMID 454290.
Sankila EM, Pakarinen H, Kääriäinen H, Aittomäki K, Karjalainen S, Sistonen P, de la Chapelle A (1995). "Assignment of Usher syndrome type III (USH3) gene to chromosome 3q". Hum. Mol. Genet. 4 (1): 93–98. doi:10.1093/hmg/4.1.93. PMID 7711740.
Hashimoto T, Gibbs D, Lillo C, Azarian SM, Legacki E, Zhang XM, Yang XJ, Williams DS (2007). "Lentiviral gene replacement therapy of retinas in a mouse model for Usher syndrome type 1B". Gene Therapy. 14 (7): 584–594. doi:10.1038/sj.gt.3302897. PMC 9307148. PMID 17268537.
Vernon M (1969). "Usher's syndrome — deafness and progressive blindness. Clinical cases, prevention, theory and literature survey". Journal of Chronic Diseases. 22 (3): 133–151. doi:10.1016/0021-9681(69)90055-1. PMID 4897966.
Boughman J, Vernon M, Shaver K (1983). "Usher syndrome: Definition and estimate of prevalence from two high-risk populations". Journal of Chronic Diseases. 36 (8): 595–603. doi:10.1016/0021-9681(83)90147-9. PMID 6885960.

fuzzywuzzydesign.com

"Who's Fuzzy". Fuzzy Wuzzy Design. Archived from the original on 2021-06-29. Retrieved 2015-08-07.

harvard.edu

ui.adsabs.harvard.edu

Libé-Philippot, Baptiste; Michel, Vincent; Monvel, Jacques Boutet de; Gal, Sébastien Le; Dupont, Typhaine; Avan, Paul; Métin, Christine; Michalski, Nicolas; Petit, Christine (2017-07-25). "Auditory cortex interneuron development requires cadherins operating hair-cell mechanoelectrical transduction". Proceedings of the National Academy of Sciences. 114 (30): 7765–7774. Bibcode:2017PNAS..114.7765L. doi:10.1073/pnas.1703408114. ISSN 0027-8424. PMC 5544301. PMID 28705869.

bertarelli.hms.harvard.edu

Dina Fine Maron (December 4, 2018). "Out of the Silence: Gene Therapy Tackles a Common Birth Defect: Deafness" (PDF). Scientific American. pp. 72–79.

nalagaat.org.il

"Nalagaat Center | Home". Archived from the original on 2010-11-24. Retrieved 2010-11-03.

nih.gov

pubmed.ncbi.nlm.nih.gov

Mets MB, Young NM, Pass A, Lasky JB (2000). "Early diagnosis of Usher syndrome in children". Transactions of the American Ophthalmological Society. 98: 237–45. PMC 1298229. PMID 11190026.
Otterstedde CR, Spandau U, Blankenagel A, Kimberling WJ, Reisser C (2001). "A new clinical classification for Usher's syndrome based on a new subtype of Usher's syndrome type I". Laryngoscope. 111 (1): 84–86. doi:10.1097/00005537-200101000-00014. PMID 11192904. S2CID 41124463.
Grøndahl J (1987). "Estimation of prognosis and prevalence of retinitis pigmentosa and Usher syndrome in Norway". Clin. Genet. 31 (4): 255–264. doi:10.1111/j.1399-0004.1987.tb02804.x. PMID 3594933. S2CID 26853136.
Pakarinen L, Tuppurainen K, Laipapala P, Mäntyjärvi M, Puhakka H (1996). "The ophthalmological course of Usher syndrome type III". International Ophthalmology. 19 (5): 307–311. doi:10.1007/BF00130927. PMID 8864816. S2CID 26501078.
Keats, Bronya J.B.; Corey, David P. (25 October 2002). "The Usher syndromes". American Journal of Medical Genetics. 89 (3): 158–166. doi:10.1002/(SICI)1096-8628(19990924)89:3<158::AID-AJMG6>3.0.CO;2-#. PMID 10704190. Retrieved 29 June 2022.
Reisser, CFV; Kimberling, WJ; Otterstedde, CR (2002). "Hearing Loss in Usher Syndrome Type II is Nonprogressive". Annals of Otology, Rhinology & Laryngology. 111 (12): 1108–1111. doi:10.1177/000348940211101208. PMID 12498372. S2CID 43346043. Retrieved 4 March 2022.
Sadeghi, Mehdi; Cohn, Edward S.; Kelly, William J.; Kimberling, William J.; Tranebjoerg, Lisbeth; Möller, Claes (2004). "Audiological findings in Usher syndrome types IIa and II (non-IIa)". International Journal of Audiology. 43 (3): 136–143. doi:10.1080/14992020400050019. PMID 15198377. S2CID 40248505.
Hope CI, Bundey S, Proops D, Fielder AR (1997). "Usher syndrome in the city of Birmingham — prevalence and clinical classification". British Journal of Ophthalmology. 81 (1): 46–53. doi:10.1136/bjo.81.1.46. PMC 1721995. PMID 9135408.
Roux AF, Faugere V, Le Guedard S, Pallares-Ruiz N, Vielle A, Chambert S, Marlin S, Hamel C, Gilbert B, Malcolm S, Claustres M (2006). "Survey of the frequency of USH1 gene mutations in a cohort of Usher patients shows the importance of cadherin 23 and protocadherin 15 genes and establishes a detection rate of above 90%". J Med Genet. 43 (9): 763–768. doi:10.1136/jmg.2006.041954. PMC 2564578. PMID 16679490.
Ouyang XM, Yan D, Du LL, Hejtmancik JF, Jacobson SG, Nance WE, Li AR, Angeli S, Kaiser M, Newton V, Brown SD, Balkany T, Liu XZ (2005). "Characterization of Usher syndrome type I gene mutations in an Usher syndrome patient population". Hum Genet. 116 (4): 292–299. doi:10.1007/s00439-004-1227-2. PMID 15660226. S2CID 22812718.
Petit, C (2001). "Usher syndrome: from genetics to pathogenesis" (PDF). Annual Review of Genomics and Human Genetics. 2: 271–97. doi:10.1146/annurev.genom.2.1.271. PMID 11701652. S2CID 505750. Archived from the original (PDF) on 2019-05-03.
Reiners, J; Nagel-Wolfrum, K; Jürgens, K; Märker, T; Wolfrum, U (2006). "Molecular basis of human Usher syndrome: deciphering the meshes of the Usher protein network provides insights into the pathomechanisms of the Usher disease" (PDF). Experimental Eye Research. 83 (1): 97–119. doi:10.1016/j.exer.2005.11.010. PMID 16545802. Archived from the original (PDF) on 2019-05-03.
Gerber, S; Bonneau, D; Gilbert, B; Munnich, A; Dufier, JL; Rozet, JM; Kaplan, J (2006). "USH1A: chronicle of a slow death". American Journal of Human Genetics. 78 (2): 357–9. doi:10.1086/500275. PMC 1380243. PMID 16400615.
Libé-Philippot, Baptiste; Michel, Vincent; Monvel, Jacques Boutet de; Gal, Sébastien Le; Dupont, Typhaine; Avan, Paul; Métin, Christine; Michalski, Nicolas; Petit, Christine (2017-07-25). "Auditory cortex interneuron development requires cadherins operating hair-cell mechanoelectrical transduction". Proceedings of the National Academy of Sciences. 114 (30): 7765–7774. Bibcode:2017PNAS..114.7765L. doi:10.1073/pnas.1703408114. ISSN 0027-8424. PMC 5544301. PMID 28705869.
Smith RJ, Berlin CI, Hejtmancik JF, Keats BJ, Kimberling WJ, Lewis RA, et al. (1994). "Clinical diagnosis of the Usher syndromes. Usher Syndrome Consortium". American Journal of Medical Genetics. 50 (1): 32–38. doi:10.1002/ajmg.1320500107. PMID 8160750.
Fishman GA, Kumar A, Joseph ME, Torok N, Andersonj RJ (1983). "Usher's syndrome: ophthalmic and neuro-otologic findings suggesting genetic heterogeneity". Archives of Ophthalmology. 101 (9): 1367–1374. doi:10.1001/archopht.1983.01040020369005. PMID 6604514.
Williams DS (2007). "Usher syndrome: Animal models, retinal function of Usher proteins, and prospects for gene therapy". Vision Research. 48 (3): 433–41. doi:10.1016/j.visres.2007.08.015. PMC 2680226. PMID 17936325.
Hammerschlag V (1907). "Zur Kenntnis der hereditaer-degenerativen Taubstummen und ihre differential diagnostische Bedeutung". Z. Ohrenheilk. 54: 18–36.
Bell J (1933). Retinitis Pigmentosa and Allied Diseases (2nd ed.). London: Cambridge University Press.
Hallgren B (1959). "Retinitis pigmentosa combined with congenital deafness with vestibulo-cerebellar ataxia and mental abnormality in a proportion of cases: Clinical and geneto-statistical survey". Acta Psychiatr Scand Suppl. 34 (138): 9–101. doi:10.1111/j.1600-0447.1959.tb08605.x. PMID 14399116. S2CID 221393918.
Merin S, Auerbach E (1976). "Retinitis pigmentosa". Surv. Ophthalmol. 20 (5): 303–345. doi:10.1016/S0039-6257(96)90001-6. PMID 817406.
Davenport S, Omenn G (1977). The Heterogeneity of Usher Syndrome (volume 426 ed.). Amsterdam: Excerpta Medica Foundation.
Gorlin R, Tilsner T, Feinstein S, Duvall AJ (1979). "Usher syndrome type III". Arch. Otolaryngol. 105 (6): 353–354. doi:10.1001/archotol.1979.00790180051011. PMID 454290.
Sankila EM, Pakarinen H, Kääriäinen H, Aittomäki K, Karjalainen S, Sistonen P, de la Chapelle A (1995). "Assignment of Usher syndrome type III (USH3) gene to chromosome 3q". Hum. Mol. Genet. 4 (1): 93–98. doi:10.1093/hmg/4.1.93. PMID 7711740.
Hashimoto T, Gibbs D, Lillo C, Azarian SM, Legacki E, Zhang XM, Yang XJ, Williams DS (2007). "Lentiviral gene replacement therapy of retinas in a mouse model for Usher syndrome type 1B". Gene Therapy. 14 (7): 584–594. doi:10.1038/sj.gt.3302897. PMC 9307148. PMID 17268537.
Vernon M (1969). "Usher's syndrome — deafness and progressive blindness. Clinical cases, prevention, theory and literature survey". Journal of Chronic Diseases. 22 (3): 133–151. doi:10.1016/0021-9681(69)90055-1. PMID 4897966.
Boughman J, Vernon M, Shaver K (1983). "Usher syndrome: Definition and estimate of prevalence from two high-risk populations". Journal of Chronic Diseases. 36 (8): 595–603. doi:10.1016/0021-9681(83)90147-9. PMID 6885960.

ncbi.nlm.nih.gov

Mets MB, Young NM, Pass A, Lasky JB (2000). "Early diagnosis of Usher syndrome in children". Transactions of the American Ophthalmological Society. 98: 237–45. PMC 1298229. PMID 11190026.
Hope CI, Bundey S, Proops D, Fielder AR (1997). "Usher syndrome in the city of Birmingham — prevalence and clinical classification". British Journal of Ophthalmology. 81 (1): 46–53. doi:10.1136/bjo.81.1.46. PMC 1721995. PMID 9135408.
Roux AF, Faugere V, Le Guedard S, Pallares-Ruiz N, Vielle A, Chambert S, Marlin S, Hamel C, Gilbert B, Malcolm S, Claustres M (2006). "Survey of the frequency of USH1 gene mutations in a cohort of Usher patients shows the importance of cadherin 23 and protocadherin 15 genes and establishes a detection rate of above 90%". J Med Genet. 43 (9): 763–768. doi:10.1136/jmg.2006.041954. PMC 2564578. PMID 16679490.
Ouyang XM, Yan D, Du LL, Hejtmancik JF, Jacobson SG, Nance WE, Li AR, Angeli S, Kaiser M, Newton V, Brown SD, Balkany T, Liu XZ (2005). "Characterization of Usher syndrome type I gene mutations in an Usher syndrome patient population". Hum Genet. 116 (4): 292–299. doi:10.1007/s00439-004-1227-2. PMID 15660226. S2CID 22812718.
Gerber, S; Bonneau, D; Gilbert, B; Munnich, A; Dufier, JL; Rozet, JM; Kaplan, J (2006). "USH1A: chronicle of a slow death". American Journal of Human Genetics. 78 (2): 357–9. doi:10.1086/500275. PMC 1380243. PMID 16400615.
Libé-Philippot, Baptiste; Michel, Vincent; Monvel, Jacques Boutet de; Gal, Sébastien Le; Dupont, Typhaine; Avan, Paul; Métin, Christine; Michalski, Nicolas; Petit, Christine (2017-07-25). "Auditory cortex interneuron development requires cadherins operating hair-cell mechanoelectrical transduction". Proceedings of the National Academy of Sciences. 114 (30): 7765–7774. Bibcode:2017PNAS..114.7765L. doi:10.1073/pnas.1703408114. ISSN 0027-8424. PMC 5544301. PMID 28705869.
Williams DS (2007). "Usher syndrome: Animal models, retinal function of Usher proteins, and prospects for gene therapy". Vision Research. 48 (3): 433–41. doi:10.1016/j.visres.2007.08.015. PMC 2680226. PMID 17936325.
Hashimoto T, Gibbs D, Lillo C, Azarian SM, Legacki E, Zhang XM, Yang XJ, Williams DS (2007). "Lentiviral gene replacement therapy of retinas in a mouse model for Usher syndrome type 1B". Gene Therapy. 14 (7): 584–594. doi:10.1038/sj.gt.3302897. PMC 9307148. PMID 17268537.

sagepub.com

journals.sagepub.com

Reisser, CFV; Kimberling, WJ; Otterstedde, CR (2002). "Hearing Loss in Usher Syndrome Type II is Nonprogressive". Annals of Otology, Rhinology & Laryngology. 111 (12): 1108–1111. doi:10.1177/000348940211101208. PMID 12498372. S2CID 43346043. Retrieved 4 March 2022.

semanticscholar.org

api.semanticscholar.org

Otterstedde CR, Spandau U, Blankenagel A, Kimberling WJ, Reisser C (2001). "A new clinical classification for Usher's syndrome based on a new subtype of Usher's syndrome type I". Laryngoscope. 111 (1): 84–86. doi:10.1097/00005537-200101000-00014. PMID 11192904. S2CID 41124463.
Grøndahl J (1987). "Estimation of prognosis and prevalence of retinitis pigmentosa and Usher syndrome in Norway". Clin. Genet. 31 (4): 255–264. doi:10.1111/j.1399-0004.1987.tb02804.x. PMID 3594933. S2CID 26853136.
Pakarinen L, Tuppurainen K, Laipapala P, Mäntyjärvi M, Puhakka H (1996). "The ophthalmological course of Usher syndrome type III". International Ophthalmology. 19 (5): 307–311. doi:10.1007/BF00130927. PMID 8864816. S2CID 26501078.
Reisser, CFV; Kimberling, WJ; Otterstedde, CR (2002). "Hearing Loss in Usher Syndrome Type II is Nonprogressive". Annals of Otology, Rhinology & Laryngology. 111 (12): 1108–1111. doi:10.1177/000348940211101208. PMID 12498372. S2CID 43346043. Retrieved 4 March 2022.
Sadeghi, Mehdi; Cohn, Edward S.; Kelly, William J.; Kimberling, William J.; Tranebjoerg, Lisbeth; Möller, Claes (2004). "Audiological findings in Usher syndrome types IIa and II (non-IIa)". International Journal of Audiology. 43 (3): 136–143. doi:10.1080/14992020400050019. PMID 15198377. S2CID 40248505.
Roux AF, Faugere V, Le Guedard S, Pallares-Ruiz N, Vielle A, Chambert S, Marlin S, Hamel C, Gilbert B, Malcolm S, Claustres M (2006). "Survey of the frequency of USH1 gene mutations in a cohort of Usher patients shows the importance of cadherin 23 and protocadherin 15 genes and establishes a detection rate of above 90%". J Med Genet. 43 (9): 763–768. doi:10.1136/jmg.2006.041954. PMC 2564578. PMID 16679490.
Ouyang XM, Yan D, Du LL, Hejtmancik JF, Jacobson SG, Nance WE, Li AR, Angeli S, Kaiser M, Newton V, Brown SD, Balkany T, Liu XZ (2005). "Characterization of Usher syndrome type I gene mutations in an Usher syndrome patient population". Hum Genet. 116 (4): 292–299. doi:10.1007/s00439-004-1227-2. PMID 15660226. S2CID 22812718.
Petit, C (2001). "Usher syndrome: from genetics to pathogenesis" (PDF). Annual Review of Genomics and Human Genetics. 2: 271–97. doi:10.1146/annurev.genom.2.1.271. PMID 11701652. S2CID 505750. Archived from the original (PDF) on 2019-05-03.
Hammerschlag V (1907). "Zur Kenntnis der hereditaer-degenerativen Taubstummen und ihre differential diagnostische Bedeutung". Z. Ohrenheilk. 54: 18–36.
Bell J (1933). Retinitis Pigmentosa and Allied Diseases (2nd ed.). London: Cambridge University Press.
Hallgren B (1959). "Retinitis pigmentosa combined with congenital deafness with vestibulo-cerebellar ataxia and mental abnormality in a proportion of cases: Clinical and geneto-statistical survey". Acta Psychiatr Scand Suppl. 34 (138): 9–101. doi:10.1111/j.1600-0447.1959.tb08605.x. PMID 14399116. S2CID 221393918.
Merin S, Auerbach E (1976). "Retinitis pigmentosa". Surv. Ophthalmol. 20 (5): 303–345. doi:10.1016/S0039-6257(96)90001-6. PMID 817406.
Davenport S, Omenn G (1977). The Heterogeneity of Usher Syndrome (volume 426 ed.). Amsterdam: Excerpta Medica Foundation.
Gorlin R, Tilsner T, Feinstein S, Duvall AJ (1979). "Usher syndrome type III". Arch. Otolaryngol. 105 (6): 353–354. doi:10.1001/archotol.1979.00790180051011. PMID 454290.

pdfs.semanticscholar.org

Petit, C (2001). "Usher syndrome: from genetics to pathogenesis" (PDF). Annual Review of Genomics and Human Genetics. 2: 271–97. doi:10.1146/annurev.genom.2.1.271. PMID 11701652. S2CID 505750. Archived from the original (PDF) on 2019-05-03.

tactiletheworld.wordpress.com

"Tactile The World". Tactile The World.

uni-mainz.de

blogs.uni-mainz.de

Reiners, J; Nagel-Wolfrum, K; Jürgens, K; Märker, T; Wolfrum, U (2006). "Molecular basis of human Usher syndrome: deciphering the meshes of the Usher protein network provides insights into the pathomechanisms of the Usher disease" (PDF). Experimental Eye Research. 83 (1): 97–119. doi:10.1016/j.exer.2005.11.010. PMID 16545802. Archived from the original (PDF) on 2019-05-03.

web.archive.org

Petit, C (2001). "Usher syndrome: from genetics to pathogenesis" (PDF). Annual Review of Genomics and Human Genetics. 2: 271–97. doi:10.1146/annurev.genom.2.1.271. PMID 11701652. S2CID 505750. Archived from the original (PDF) on 2019-05-03.
Reiners, J; Nagel-Wolfrum, K; Jürgens, K; Märker, T; Wolfrum, U (2006). "Molecular basis of human Usher syndrome: deciphering the meshes of the Usher protein network provides insights into the pathomechanisms of the Usher disease" (PDF). Experimental Eye Research. 83 (1): 97–119. doi:10.1016/j.exer.2005.11.010. PMID 16545802. Archived from the original (PDF) on 2019-05-03.
"Who's Fuzzy". Fuzzy Wuzzy Design. Archived from the original on 2021-06-29. Retrieved 2015-08-07.
"Nalagaat Center | Home". Archived from the original on 2010-11-24. Retrieved 2010-11-03.

wiley.com

onlinelibrary.wiley.com

Keats, Bronya J.B.; Corey, David P. (25 October 2002). "The Usher syndromes". American Journal of Medical Genetics. 89 (3): 158–166. doi:10.1002/(SICI)1096-8628(19990924)89:3<158::AID-AJMG6>3.0.CO;2-#. PMID 10704190. Retrieved 29 June 2022.

worldcat.org

search.worldcat.org

Libé-Philippot, Baptiste; Michel, Vincent; Monvel, Jacques Boutet de; Gal, Sébastien Le; Dupont, Typhaine; Avan, Paul; Métin, Christine; Michalski, Nicolas; Petit, Christine (2017-07-25). "Auditory cortex interneuron development requires cadherins operating hair-cell mechanoelectrical transduction". Proceedings of the National Academy of Sciences. 114 (30): 7765–7774. Bibcode:2017PNAS..114.7765L. doi:10.1073/pnas.1703408114. ISSN 0027-8424. PMC 5544301. PMID 28705869.