Berlin CI - Search Results

1

Clinical diagnosis of the Usher syndromes. Usher Syndrome Consortium.

Smith RJ, Berlin CI, Hejtmancik JF, Keats BJ, Kimberling WJ, Lewis RA, Möller CG, Pelias MZ, Tranebjaerg L. Smith RJ, et al. Among authors: berlin ci. Am J Med Genet. 1994 Mar 1;50(1):32-8. doi: 10.1002/ajmg.1320500107. Am J Med Genet. 1994. PMID: 8160750

2

OTOF mutations revealed by genetic analysis of hearing loss families including a potential temperature sensitive auditory neuropathy allele.

Varga R, Avenarius MR, Kelley PM, Keats BJ, Berlin CI, Hood LJ, Morlet TG, Brashears SM, Starr A, Cohn ES, Smith RJ, Kimberling WJ. Varga R, et al. Among authors: berlin ci. J Med Genet. 2006 Jul;43(7):576-81. doi: 10.1136/jmg.2005.038612. Epub 2005 Dec 21. J Med Genet. 2006. PMID: 16371502 Free PMC article.

3

Genomics and hearing impairment.

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

4

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

5

Autosomal recessive nonsyndromic neurosensory deafness at DFNB1 not associated with the compound-heterozygous GJB2 (connexin 26) genotype M34T/167delT.

Griffith AJ, Chowdhry AA, Kurima K, Hood LJ, Keats B, Berlin CI, Morell RJ, Friedman TB. Griffith AJ, et al. Among authors: berlin ci. Am J Hum Genet. 2000 Sep;67(3):745-9. doi: 10.1086/303045. Epub 2000 Jul 19. Am J Hum Genet. 2000. PMID: 10903123 Free PMC article.

6

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: berlin ci. Hear Res. 1996 Sep 1;98(1-2):18-21. doi: 10.1016/0378-5955(96)00041-x. Hear Res. 1996. PMID: 8880177

7

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: berlin ci. Hear Res. 1998 Mar;117(1-2):24-30. doi: 10.1016/s0378-5955(98)00005-7. Hear Res. 1998. PMID: 9557975

8

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: berlin ci. Hear Res. 1995 Aug;88(1-2):61-4. doi: 10.1016/0378-5955(95)00099-p. Hear Res. 1995. PMID: 8576004

9

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. Among authors: berlin ci. Mamm Genome. 1995 Jan;6(1):8-10. doi: 10.1007/BF00350886. Mamm Genome. 1995. PMID: 7719036

10

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: berlin ci. 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.

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