Weston MD - Search Results

1

Phylogenetic analysis of mitochondrial DNA in Japanese pedigrees of sensorineural hearing loss associated with the A1555G mutation.

Abe S, Usami S, Shinkawa H, Weston MD, Overbeck LD, Hoover DM, Kenyon JB, Horai S, Kimberling WJ. Abe S, et al. Among authors: weston md. Eur J Hum Genet. 1998 Nov-Dec;6(6):563-9. doi: 10.1038/sj.ejhg.5200239. Eur J Hum Genet. 1998. PMID: 9887373

2

Non-syndromic hearing loss associated with enlarged vestibular aqueduct is caused by PDS mutations.

Usami S, Abe S, Weston MD, Shinkawa H, Van Camp G, Kimberling WJ. Usami S, et al. Among authors: weston md. Hum Genet. 1999 Feb;104(2):188-92. doi: 10.1007/s004390050933. Hum Genet. 1999. PMID: 10190331

3

Myosin VIIA mutation screening in 189 Usher syndrome type 1 patients.

Weston MD, Kelley PM, Overbeck LD, Wagenaar M, Orten DJ, Hasson T, Chen ZY, Corey D, Mooseker M, Sumegi J, Cremers C, Moller C, Jacobson SG, Gorin MB, Kimberling WJ. Weston MD, et al. Am J Hum Genet. 1996 Nov;59(5):1074-83. Am J Hum Genet. 1996. PMID: 8900236 Free PMC article.

4

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. 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.

5

Identification of novel USH2A mutations: implications for the structure of USH2A protein.

Dreyer B, Tranebjaerg L, Rosenberg T, Weston MD, Kimberling WJ, Nilssen O. Dreyer B, et al. Among authors: weston md. Eur J Hum Genet. 2000 Jul;8(7):500-6. doi: 10.1038/sj.ejhg.5200491. Eur J Hum Genet. 2000. PMID: 10909849

6

USH2A mutation analysis in 70 Dutch families with Usher syndrome type II.

Pennings RJ, Te Brinke H, Weston MD, Claassen A, Orten DJ, Weekamp H, Van Aarem A, Huygen PL, Deutman AF, Hoefsloot LH, Cremers FP, Cremers CW, Kimberling WJ, Kremer H. Pennings RJ, et al. Among authors: weston md. Hum Mutat. 2004 Aug;24(2):185. doi: 10.1002/humu.9259. Hum Mutat. 2004. PMID: 15241801

7

Dinucleotide repeat polymorphism for D1S70 (CRI-L461) on chromosome 1q41.

Weston MD, Kimberling WJ. Weston MD, et al. Hum Mol Genet. 1994 Jul;3(7):1212. doi: 10.1093/hmg/3.7.1212. Hum Mol Genet. 1994. PMID: 7981712 No abstract available.

8

Erratum: analysis of DNA elements that modulate myosin VIIa expression in humans.

Orten DJ, Weston MD, Kelley PM, Cremers CW, Wagenaar M, Jacobson SG, Kimberling WJ. Orten DJ, et al. Among authors: weston md. Hum Mutat. 2000 Jan;15(1):114-5. doi: 10.1002/(SICI)1098-1004(200001)15:1<114::AID-HUMU21>3.0.CO;2-4. Hum Mutat. 2000. PMID: 10612833

9

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: weston md. Am J Hum Genet. 1995 Jan;56(1):216-23. Am J Hum Genet. 1995. PMID: 7825581 Free PMC article.

10

Dinucleotide (CT)n (CA)n repeat polymorphism for D11S787 on chromosome 11q13.4.

Overbeck LD, Weston MD, Kimberling WJ, Evans GA. Overbeck LD, et al. Among authors: weston md. Hum Mol Genet. 1993 May;2(5):611. doi: 10.1093/hmg/2.5.611. Hum Mol Genet. 1993. PMID: 8518805 No abstract available.

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