Martini A - Search Results

1

Localization of Usher syndrome type II to chromosome 1q.

Kimberling WJ, Weston MD, Möller C, Davenport SL, Shugart YY, Priluck IA, Martini A, Milani M, Smith RJ. Kimberling WJ, et al. Among authors: martini a. Genomics. 1990 Jun;7(2):245-9. doi: 10.1016/0888-7543(90)90546-7. Genomics. 1990. PMID: 2347588

2

Genomic structure and identification of novel mutations in usherin, the gene responsible for Usher syndrome type IIa.

Weston MD, Eudy JD, Fujita S, Yao S, Usami S, Cremers C, Greenberg J, Ramesar R, Martini A, Moller C, Smith RJ, Sumegi J, Kimberling WJ. Weston MD, et al. Among authors: martini a. Am J Hum Genet. 2000 Apr;66(4):1199-210. doi: 10.1086/302855. Epub 2000 Mar 22. Am J Hum Genet. 2000. PMID: 10729113 Free PMC article.

3

Genetic studies of Usher syndrome.

Kimberling WJ, Weston MD, Pieke Dahl S, Kenyon JB, Shugart YY, Moller C, Davenport SL, Martini A, Milani M, Smith RJ. Kimberling WJ, et al. Among authors: martini a. Ann N Y Acad Sci. 1991;630:167-75. doi: 10.1111/j.1749-6632.1991.tb19585.x. Ann N Y Acad Sci. 1991. PMID: 1952588 No abstract available.

4

A progress report on the localization of Usher syndrome type II to chromosome 1q.

Weston MD, Kimberling WJ, Möller CG, Pieke Dahl S, Smith RJ, Martini A, Milani M. Weston MD, et al. Among authors: martini a. Ann N Y Acad Sci. 1991;630:284-7. doi: 10.1111/j.1749-6632.1991.tb19606.x. Ann N Y Acad Sci. 1991. PMID: 1952607 No abstract available.

5

Gene mapping of Usher syndrome type IIa: localization of the gene to a 2.1-cM segment on chromosome 1q41.

Kimberling WJ, Weston MD, Möller C, van Aarem A, Cremers CW, Sumegi J, Ing PS, Connolly C, Martini A, Milani M, et al. Kimberling WJ, et al. Among authors: martini a. Am J Hum Genet. 1995 Jan;56(1):216-23. Am J Hum Genet. 1995. PMID: 7825581 Free PMC article.

6

An introduction to the genetics of normal and defective hearing.

Martini A, Mazzoli M, Kimberling W. Martini A, et al. Ann N Y Acad Sci. 1997 Dec 29;830:361-74. doi: 10.1111/j.1749-6632.1997.tb51908.x. Ann N Y Acad Sci. 1997. PMID: 9616696 Review.

7

Audiometric patterns of genetic non-syndromal sensorineural hearing loss.

Martini A, Milani M, Rosignoli M, Mazzoli M, Prosser S. Martini A, et al. Audiology. 1997 Jul-Aug;36(4):228-36. doi: 10.3109/00206099709071975. Audiology. 1997. PMID: 9253481

8

Auditory and academic performance of children with unilateral hearing loss.

Bovo R, Martini A, Agnoletto M, Beghi A, Carmignoto D, Milani M, Zangaglia AM. Bovo R, et al. Among authors: martini a. Scand Audiol Suppl. 1988;30:71-4. Scand Audiol Suppl. 1988. PMID: 3227285

9

Mapping of a new autosomal dominant non-syndromic hearing loss locus (DFNA43) to chromosome 2p12.

Flex E, Mangino M, Mazzoli M, Martini A, Migliosi V, Colosimo A, Mingarelli R, Pizzuti A, Dallapiccola B. Flex E, et al. Among authors: martini a. J Med Genet. 2003 Apr;40(4):278-81. doi: 10.1136/jmg.40.4.278. J Med Genet. 2003. PMID: 12676899 Free PMC article.

10

Molecular epidemiology of Usher syndrome in Italy.

Vozzi D, Aaspõllu A, Athanasakis E, Berto A, Fabretto A, Licastro D, Külm M, Testa F, Trevisi P, Vahter M, Ziviello C, Martini A, Simonelli F, Banfi S, Gasparini P. Vozzi D, et al. Among authors: martini a. Mol Vis. 2011;17:1662-8. Epub 2011 Jun 22. Mol Vis. 2011. PMID: 21738395 Free PMC article.

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