Ross DA - Search Results

1

Regional chromosomal assignment of human renin gene to 1q12----qter and use in linkage studies in Charcot-Marie-Tooth disease.

Griffiths LR, Nicholson GA, Ross DA, Zwi MB, McLeod JG, Mohandas T, Morris BJ. Griffiths LR, et al. Among authors: ross da. Cytogenet Cell Genet. 1987;45(3-4):231-3. doi: 10.1159/000132459. Cytogenet Cell Genet. 1987. PMID: 3319438

2

Charcot-Marie-Tooth neuropathy type 1A mutation: apparent crossovers with D17S122 are due to a duplication.

Nicholson GA, Kennerson ML, Keats BJ, Mesterovic N, Churcher W, Barker D, Ross DA. Nicholson GA, et al. Among authors: ross da. Am J Med Genet. 1992 Nov 1;44(4):455-60. doi: 10.1002/ajmg.1320440414. Am J Med Genet. 1992. PMID: 1442887

3

Isolation and use of chromosome 1 probes for linkage studies on Charcot-Marie-Tooth disease.

Griffiths LR, Zwi MB, Mesterovic N, Ross DA, Board PG, Callen DF, Mohandas T, Buckland R, Fletcher JM, Driesel AJ. Griffiths LR, et al. Among authors: ross da. Ann Hum Genet. 1990 Jan;54(1):31-7. doi: 10.1111/j.1469-1809.1990.tb00358.x. Ann Hum Genet. 1990. PMID: 2321912

4

Heterogeneity evidence and linkage studies on Charcot-Marie-Tooth disease.

Griffiths LR, Zwi MB, McLeod JG, Ross DA, Nicholson GA. Griffiths LR, et al. Among authors: ross da. Neurology. 1989 Feb;39(2 Pt 1):280-1. doi: 10.1212/wnl.39.2.280. Neurology. 1989. PMID: 2915802

5

A frame shift mutation in the PMP22 gene in hereditary neuropathy with liability to pressure palsies.

Nicholson GA, Valentijn LJ, Cherryson AK, Kennerson ML, Bragg TL, DeKroon RM, Ross DA, Pollard JD, McLeod JG, Bolhuis PA, et al. Nicholson GA, et al. Among authors: ross da. Nat Genet. 1994 Mar;6(3):263-6. doi: 10.1038/ng0394-263. Nat Genet. 1994. PMID: 8012388

6

A chromosome 1 BglI RFLP for the LR67 anonymous DNA segment [D1S26].

Griffiths LR, Ross DA, Mesterovic N, McLeod JG, Nicholson GA. Griffiths LR, et al. Among authors: ross da. Nucleic Acids Res. 1988 Aug 11;16(15):7752. doi: 10.1093/nar/16.15.7752. Nucleic Acids Res. 1988. PMID: 2901066 Free PMC article. No abstract available.

7

The peripheral myelin gene PMP-22/GAS-3 is duplicated in Charcot-Marie-Tooth disease type 1A.

Valentijn LJ, Bolhuis PA, Zorn I, Hoogendijk JE, van den Bosch N, Hensels GW, Stanton VP Jr, Housman DE, Fischbeck KH, Ross DA, et al. Valentijn LJ, et al. Among authors: ross da. Nat Genet. 1992 Jun;1(3):166-70. doi: 10.1038/ng0692-166. Nat Genet. 1992. PMID: 1303229

8

DNA testing in familial hypertrophic cardiomyopathy: clinical and laboratory implications.

Smart RV, Yu B, Le H, French JA, Richmond DR, Jeremy RW, Semsarian C, Cheung L, Ross DA, Trent RJ. Smart RV, et al. Among authors: ross da. Clin Genet. 1996 Oct;50(4):169-75. doi: 10.1111/j.1399-0004.1996.tb02621.x. Clin Genet. 1996. PMID: 9001794

9

Localization of a gene for incomplete X-linked congenital stationary night blindness to the interval between DXS6849 and DXS8023 in Xp11.23.

Bech-Hansen NT, Boycott KM, Gratton KJ, Ross DA, Field LL, Pearce WG. Bech-Hansen NT, et al. Among authors: ross da. Hum Genet. 1998 Aug;103(2):124-30. doi: 10.1007/s004390050794. Hum Genet. 1998. PMID: 9760193

10

Minimally Invasive Cervical Synovial Cyst Resection: 2-Dimensional Operative Video.

Gragg AL, Ross DA. Gragg AL, et al. Among authors: ross da. Oper Neurosurg (Hagerstown). 2024 Dec 20. doi: 10.1227/ons.0000000000001479. Online ahead of print. Oper Neurosurg (Hagerstown). 2024. PMID: 39704518 No abstract available.

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