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" Usher syndrome ID and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23. Am J Hum Genet 2001;68:26-37. "
Adler Fisiología Del Ojo: Aplicación Clínica - Página 370
editado por - 2003 - 906 páginas
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Genetic Hearing Impairment: Its Clinical Presentations

Cornelius Wilhelmus Radboud Jozef Cremers, Richard Smith - 2002 - 263 páginas
...Bitner-Glindizicz M, Nance WE, Liu XZ, Wistow G, Smith RJH, Griffith AJ, Wilcox ER, Friedman TB, Morell RJ: Usher syndrome ID and nonsyndromic autosomal recessive...the novel cadherin-like gene CDH23. Am J Hum Genet 2001;68:26-37. 5 Bolz H, von Brederlow B, Ramirez A, Bryda EC, Kutsche K, Nothwang HG, Seeliger M,...
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Photoreceptors and Calcium

Wolfgang Baehr, Krzysztof Palczewski - 2003 - 658 páginas
...Peters LM, Riazuddin S et at. Usher syndrome lD and nonsyndromic autosomal recessive deafness DFNBI2 are caused by allelic mutations of the novel cadherin-like gene CDH23. Am J Hum Genet 2001; 68(l):26-37. 20. Di Palma F, Holme RH, Bryda EC at al. Mutations in Cdh23, encoding a new type...
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Genetic Hearing Loss

Patrick J. Willems - 2003 - 508 páginas
...member of the cadherin gene family, causes Usher syndrome type ID. Nat Genet 2001; 27(1):108-112. 11. Bork JM, et al. Usher syndrome ID and nonsyndromic...the novel cadherin-like gene CDH23. Am J Hum Genet 2001; 68(1):26-37. 12. Chaib H, et al. A newly identified locus for Usher syndrome type I, USH1E, maps...
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Genetics in Ophthalmology

B. Wissinger, Susanne Kohl, U. Langenbeck - 2003 - 230 páginas
...Bitner-Glindzicz M, Nance WE, Liu XZ, Wistow G, Smith RJH, Griffith AJ, Wilcox ER, Friedman TB, Morell RJ: Usher syndrome ID and nonsyndromic autosomal recessive...the novel cadherin-like gene CDH23. Am J Hum Genet 2001;68:26-37. 33 Alagramam KN, Yuan H, Kuehn MH, Murcia CL, Wayne S, Srisailpathy CR, Lowry RB, Knaus...
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Development of Auditory and Vestibular Systems-3: Molecular Development of ...

Raymond Romand, Isabel Varela-Nieto - 2003 - 490 páginas
...Bernstein, SL, Ahmed, ZM, Ness, SL, Polomeno, R., Ramesh, A., Schloss, M., Srisailpathy, CR, et al. (2001). Usher syndrome ID and nonsyndromic autosomal recessive...novel cadherin-like gene CDH23. Am. J. Hum. Genet. 68, 26-37. Bowen, MA, Patel, DD, Li, X., Modrell, B., Malacko, AR, Wang, WC, Marquardt, H., Neubauer,...
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Hipocausia Neurosensorial

L Vallejo Valdezate - 2003 - 208 páginas
...165-172. 28. Bork JM, Peters LM, Riazuddin S, Bernstein SL, Ahmed ZM, Ness SL y cols. Usher syndrome l D and nonsyndromic autosomal recessive deafness DFNB12...the novel cadherin-like gene CDH23. Am J Hum Genet 200 1; 68: 26-37. 29. Di Palma F, Holme RH, Bryda EC, Belyantseva IA, Pellegrino R y cols. Mutations...
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Pediatric Retina

Mary Elizabeth Hartnett - 2005 - 582 páginas
...complexes. Annu Rev Neurosa 2001 ;24:1-29. 47. Bork JM, Peters LM, Riazuddin S, et al. Usher syndrome l D and nonsyndromic autosomal recessive deafness DFNB12...the novel cadherin-like gene CDH23. Am J Hum Genet 2001 ;68:26-37. 48. Bolz H, von Brederlow B, Ramirez A, et al. Mutation of CDH23, encoding a new member...
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Development of the Inner Ear

Matthew Kelley - 2005 - 264 páginas
...Bitner-Glindzicz M, Nance WE, Liu XZ, Wistow G, Smith RJ, Griffith AJ, Wilcox ER, Friedman TB, Morell RJ (2001) Usher syndrome ID and nonsyndromic autosomal recessive...the novel cadherin-like gene CDH23. Am J Hum Genet 68:26-37. Borsani G, DeGrandi A, Ballabio A, Bulfone A, Bernard L, Banfi S, Gattuso C, Mariani M, Dixon...
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Molecular Motors

Manfred Schliwa - 2006 - 604 páginas
...causes Usher syndrome type 1D. Nature Genet. 27: 108-112. Bork, JM, et al., 2001. Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12...novel cadherin-like gene CDH23. Am. J. Hum. Genet. 68: 26-37. Breckler, J., K. Au, J. Cheng, T. Hasson and B. Burnside. 2000. Novel myosin VI isoform...
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Genes, Hearing, and Deafness: From Molecular Biology to Clinical Practice

Alessandro Martini, Dafydd Stephens, Andrew P. Read - 2007 - 338 páginas
...links in zebrafish sensory hair cells. Nature 2004; 428: 955-959. 69. Bork JM, Peters LM, Riazuddin S, et al. Usher syndrome ID and nonsyndromic autosomal...the novel cadherin-like gene CDH23. Am J Hum Genet 2001; 68:26-37. 70. Di Palma F, Holme RH, Bryda EC, et al. Mutations in Cdh23, encoding a new type...
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