Keats BJ - Search Results

1

The deafness locus (dn) maps to mouse chromosome 19.

Keats BJ, Nouri N, Huang JM, Money M, Webster DB, Berlin CI. Keats BJ, et al. Mamm Genome. 1995 Jan;6(1):8-10. doi: 10.1007/BF00350886. Mamm Genome. 1995. PMID: 7719036

2

A locus for axonal motor-sensory neuropathy with deafness and mental retardation maps to Xq24-q26.

Priest JM, Fischbeck KH, Nouri N, Keats BJ. Priest JM, et al. Among authors: keats bj. Genomics. 1995 Sep 20;29(2):409-12. doi: 10.1006/geno.1995.9987. Genomics. 1995. PMID: 8666389 Free article.

3

The mouse deafness locus (dn) is associated with an inversion on chromosome 19.

Viñas AM, Drury SS, DeAngelis MM, Den Z, Huang JM, Berlin CI, Hunt JD, Batzer MA, Deininger PL, Keats BJ. Viñas AM, et al. Among authors: keats bj. Biochim Biophys Acta. 1998 Sep 30;1407(3):257-62. doi: 10.1016/s0925-4439(98)00050-7. Biochim Biophys Acta. 1998. PMID: 9748617 Free article.

4

Auditory phenotyping of heterozygous sound-responsive (+/dn) and deafness (dn/dn) mice.

Huang JM, Money MK, Berlin CI, Keats BJ. Huang JM, et al. Among authors: keats bj. Hear Res. 1995 Aug;88(1-2):61-4. doi: 10.1016/0378-5955(95)00099-p. Hear Res. 1995. PMID: 8576004

5

Genomics and hearing impairment.

Keats BJ, Berlin CI. Keats BJ, et al. Genome Res. 1999 Jan;9(1):7-16. Genome Res. 1999. PMID: 9927480 Free article. Review.

6

Tightly linked flanking microsatellite markers for the Usher syndrome type I locus on the short arm of chromosome 11.

Keats BJ, Nouri N, Pelias MZ, Deininger PL, Litt M. Keats BJ, et al. Am J Hum Genet. 1994 Apr;54(4):681-6. Am J Hum Genet. 1994. PMID: 8128966 Free PMC article.

7

Phenotypic patterns of distortion product otoacoustic emission in inbred and F1 hybrid hearing mouse strains.

Huang JM, Money MK, Berlin CI, Keats BJ. Huang JM, et al. Among authors: keats bj. Hear Res. 1996 Sep 1;98(1-2):18-21. doi: 10.1016/0378-5955(96)00041-x. Hear Res. 1996. PMID: 8880177

8

Low intensities and 1.3 ratio produce distortion product otoacoustic emissions which are larger in heterozygous (+/dn) than homozygous (+/+) mice.

Huang JM, Berlin CI, Lin ST, Keats BJ. Huang JM, et al. Among authors: keats bj. Hear Res. 1998 Mar;117(1-2):24-30. doi: 10.1016/s0378-5955(98)00005-7. Hear Res. 1998. PMID: 9557975

9

Connexin 26 variants and auditory neuropathy/dys-synchrony among children in schools for the deaf.

Cheng X, Li L, Brashears S, Morlet T, Ng SS, Berlin C, Hood L, Keats B. Cheng X, et al. Am J Med Genet A. 2005 Nov 15;139(1):13-8. doi: 10.1002/ajmg.a.30929. Am J Med Genet A. 2005. PMID: 16222667

10

Multi-site diagnosis and management of 260 patients with auditory neuropathy/dys-synchrony (auditory neuropathy spectrum disorder).

Berlin CI, Hood LJ, Morlet T, Wilensky D, Li L, Mattingly KR, Taylor-Jeanfreau J, Keats BJ, John PS, Montgomery E, Shallop JK, Russell BA, Frisch SA. Berlin CI, et al. Among authors: keats bj. Int J Audiol. 2010 Jan;49(1):30-43. doi: 10.3109/14992020903160892. Int J Audiol. 2010. PMID: 20053155

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