Chance PF - Search Results

1

Hereditary neuralgic amyotrophy: evidence for genetic homogeneity and mapping to chromosome 17q25.

Pellegrino JE, George RA, Biegel J, Farlow MR, Gardner K, Caress J, Brown MJ, Rebbeck TR, Bird TD, Chance PF. Pellegrino JE, et al. Among authors: chance pf. Hum Genet. 1997 Dec;101(3):277-83. doi: 10.1007/s004390050629. Hum Genet. 1997. PMID: 9439655

2

Duplication within the SEPT9 gene associated with a founder effect in North American families with hereditary neuralgic amyotrophy.

Landsverk ML, Ruzzo EK, Mefford HC, Buysse K, Buchan JG, Eichler EE, Petty EM, Peterson EA, Knutzen DM, Barnett K, Farlow MR, Caress J, Parry GJ, Quan D, Gardner KL, Hong M, Simmons Z, Bird TD, Chance PF, Hannibal MC. Landsverk ML, et al. Among authors: chance pf. Hum Mol Genet. 2009 Apr 1;18(7):1200-8. doi: 10.1093/hmg/ddp014. Epub 2009 Jan 12. Hum Mol Genet. 2009. PMID: 19139049 Free PMC article.

3

Hereditary neuralgic amyotrophy and hereditary neuropathy with liability to pressure palsies: two distinct genetic disorders.

Chance PF, Lensch MW, Lipe H, Brown RH Sr, Brown RH Jr, Bird TD. Chance PF, et al. Neurology. 1994 Dec;44(12):2253-7. doi: 10.1212/wnl.44.12.2253. Neurology. 1994. PMID: 7991108

4

Mapping of hereditary neuralgic amyotrophy (familial brachial plexus neuropathy) to distal chromosome 17q.

Pellegrino JE, Rebbeck TR, Brown MJ, Bird TD, Chance PF. Pellegrino JE, et al. Among authors: chance pf. Neurology. 1996 Apr;46(4):1128-32. doi: 10.1212/wnl.46.4.1128. Neurology. 1996. PMID: 8780104

5

Craniofacial and cutaneous findings expand the phenotype of hereditary neuralgic amyotrophy.

Jeannet PY, Watts GD, Bird TD, Chance PF. Jeannet PY, et al. Among authors: chance pf. Neurology. 2001 Dec 11;57(11):1963-8. doi: 10.1212/wnl.57.11.1963. Neurology. 2001. PMID: 11739810

6

Mapping of Charcot-Marie-Tooth disease type 1C to chromosome 16p identifies a novel locus for demyelinating neuropathies.

Street VA, Goldy JD, Golden AS, Tempel BL, Bird TD, Chance PF. Street VA, et al. Among authors: chance pf. Am J Hum Genet. 2002 Jan;70(1):244-50. doi: 10.1086/337943. Epub 2001 Nov 16. Am J Hum Genet. 2002. PMID: 11713717 Free PMC article.

7

Mutations in SEPT9 cause hereditary neuralgic amyotrophy.

Kuhlenbäumer G, Hannibal MC, Nelis E, Schirmacher A, Verpoorten N, Meuleman J, Watts GD, De Vriendt E, Young P, Stögbauer F, Halfter H, Irobi J, Goossens D, Del-Favero J, Betz BG, Hor H, Kurlemann G, Bird TD, Airaksinen E, Mononen T, Serradell AP, Prats JM, Van Broeckhoven C, De Jonghe P, Timmerman V, Ringelstein EB, Chance PF. Kuhlenbäumer G, et al. Among authors: chance pf. Nat Genet. 2005 Oct;37(10):1044-6. doi: 10.1038/ng1649. Epub 2005 Sep 25. Nat Genet. 2005. PMID: 16186812

8

Chromosome 1 Charcot-Marie-Tooth disease (CMT1B) locus in the Fc gamma receptor gene region.

Lebo RV, Chance PF, Dyck PJ, Redila-Flores MT, Lynch ED, Golbus MS, Bird TD, King MC, Anderson LA, Hall J, et al. Lebo RV, et al. Among authors: chance pf. Hum Genet. 1991 Nov;88(1):1-12. doi: 10.1007/BF00204921. Hum Genet. 1991. PMID: 1683643

9

Multicolor in situ hybridization and linkage analysis order Charcot-Marie-Tooth type I (CMTIA) gene-region markers.

Lebo RV, Lynch ED, Bird TD, Golbus MS, Barker DF, O'Connell P, Chance PF. Lebo RV, et al. Among authors: chance pf. Am J Hum Genet. 1992 Jan;50(1):42-55. Am J Hum Genet. 1992. PMID: 1729894 Free PMC article.

10

Genetic linkage and heterogeneity in type I Charcot-Marie-Tooth disease (hereditary motor and sensory neuropathy type I).

Chance PF, Bird TD, O'Connell P, Lipe H, Lalouel JM, Leppert M. Chance PF, et al. Am J Hum Genet. 1990 Dec;47(6):915-25. Am J Hum Genet. 1990. PMID: 2239969 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

108 results

Search Page

Filters