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Items: 1 to 20 of 192

1.

Confirmation of linkage of type 1 hereditary sensory neuropathy to human chromosome 9q22.

Bejaoui K, McKenna-Yasek D, Hosler BA, Burns-Deater E, Deater LM, O'Neill G, Haines JL, Brown RH Jr.

Neurology. 1999 Feb;52(3):510-5.

PMID:
10025779
3.

The gene for hereditary sensory neuropathy type I (HSN-I) maps to chromosome 9q22.1-q22.3.

Nicholson GA, Dawkins JL, Blair IP, Kennerson ML, Gordon MJ, Cherryson AK, Nash J, Bananis T.

Nat Genet. 1996 May;13(1):101-4.

PMID:
8673084
4.
5.

Ulcero-mutilating neuropathy in an Austrian kinship without linkage to hereditary motor and sensory neuropathy IIB and hereditary sensory neuropathy I loci.

Auer-Grumbach M, Wagner K, Timmerman V, De Jonghe P, Hartung HP.

Neurology. 2000 Jan 11;54(1):45-52.

PMID:
10636124
6.

A locus for hereditary sensory neuropathy with cough and gastroesophageal reflux on chromosome 3p22-p24.

Kok C, Kennerson ML, Spring PJ, Ing AJ, Pollard JD, Nicholson GA.

Am J Hum Genet. 2003 Sep;73(3):632-7. Epub 2003 Jul 17.

7.

Autosomal dominant hereditary sensory neuropathy with chronic cough and gastro-oesophageal reflux: clinical features in two families linked to chromosome 3p22-p24.

Spring PJ, Kok C, Nicholson GA, Ing AJ, Spies JM, Bassett ML, Cameron J, Kerlin P, Bowler S, Tuck R, Pollard JD.

Brain. 2005 Dec;128(Pt 12):2797-810.

8.

A family with autosomal dominant mutilating neuropathy not linked to either Charcot-Marie-Tooth disease type 2B (CMT2B) or hereditary sensory neuropathy type I (HSN I) loci.

Bellone E, Rodolico C, Toscano A, Di Maria E, Cassandrini D, Pizzuti A, Pigullo S, Mazzeo A, Macaione V, Girlanda P, Vita G, Ajmar F, Mandich P.

Neuromuscul Disord. 2002 Mar;12(3):286-91.

PMID:
11801401
9.

SPTLC1 mutation in twin sisters with hereditary sensory neuropathy type I.

Verhoeven K, Coen K, De Vriendt E, Jacobs A, Van Gerwen V, Smouts I, Pou-Serradell A, Martin JJ, Timmerman V, De Jonghe P.

Neurology. 2004 Mar 23;62(6):1001-2.

PMID:
15037712
10.

Exclusion of p75NGFR and other candidate genes in a family with hereditary sensory neuropathy type II.

Davar G, Shalish C, Blumenfeld A, Breakfield XO.

Pain. 1996 Sep;67(1):135-9.

PMID:
8895241
11.

Refined localization of the cerebral cavernous malformation gene (CCM1) to a 4-cM interval of chromosome 7q contained in a well-defined YAC contig.

Johnson EW, Iyer LM, Rich SS, Orr HT, Gil-Nagel A, Kurth JH, Zabramski JM, Marchuk DA, Weissenbach J, Clericuzio CL, Davis LE, Hart BL, Gusella JF, Kosofsky BE, Louis DN, Morrison LA, Green ED, Weber JL.

Genome Res. 1995 Nov;5(4):368-80.

12.

Construction of a yeast artificial chromosome contig spanning the spinal muscular atrophy disease gene region.

Kleyn PW, Wang CH, Lien LL, Vitale E, Pan J, Ross BM, Grunn A, Palmer DA, Warburton D, Brzustowicz LM, et al.

Proc Natl Acad Sci U S A. 1993 Jul 15;90(14):6801-5.

13.

Genetic refinement and physical mapping of a 2.3 Mb probable disease region associated with a bipolar affective disorder susceptibility locus on chromosome 4q35.

Badenhop RF, Moses MJ, Scimone A, Adams LJ, Kwok JB, Jones AM, Davison G, Evans MR, Kirkby KC, Hewitt JE, Donald JA, Mitchell PB, Schofield PR.

Am J Med Genet B Neuropsychiatr Genet. 2003 Feb;117B(1):23-32.

PMID:
12555231
14.

Autosomal recessive mutilating sensory neuropathy with spastic paraplegia maps to chromosome 5p15.31-14.1.

Bouhouche A, Benomar A, Bouslam N, Ouazzani R, Chkili T, Yahyaoui M.

Eur J Hum Genet. 2006 Feb;14(2):249-52.

15.

Refinement of a locus for Marie Unna hereditary hypotrichosis to a 1.1-cM interval at 8p21.3.

He PP, Zhang XJ, Yang Q, Li M, Liang YH, Yang S, Yan KL, Cui Y, Shen YY, Wang HY, Sun LD, Du WH, Shen YJ, Xu SJ, Huang W.

Br J Dermatol. 2004 May;150(5):837-42.

PMID:
15149494
16.

Autosomal dominant sensory/motor neuropathy with Ataxia (SMNA): Linkage to chromosome 7q22-q32.

Brkanac Z, Fernandez M, Matsushita M, Lipe H, Wolff J, Bird TD, Raskind WH.

Am J Med Genet. 2002 May 8;114(4):450-7.

PMID:
11992570
17.

Mutilating neuropathic ulcerations in a chromosome 3q13-q22 linked Charcot-Marie-Tooth disease type 2B family.

De Jonghe P, Timmerman V, FitzPatrick D, Spoelders P, Martin JJ, Van Broeckhoven C.

J Neurol Neurosurg Psychiatry. 1997 Jun;62(6):570-3.

18.

Characterization of a YAC contig containing the NBCCS locus and a novel Kruppel-type zinc finger sequence on chromosome segment 9q22.3.

Chidambaram A, Gailani M, Gerrard B, Stewart C, Goldstein A, Chumakov I, Bale AE, Dean M.

Genes Chromosomes Cancer. 1997 Mar;18(3):212-8.

PMID:
9071574
19.

CORD9 a new locus for arCRD: mapping to 8p11, estimation of frequency, evaluation of a candidate gene.

Danciger M, Hendrickson J, Lyon J, Toomes C, McHale JC, Fishman GA, Inglehearn CF, Jacobson SG, Farber DB.

Invest Ophthalmol Vis Sci. 2001 Oct;42(11):2458-65.

PMID:
11581183
20.

Linkage analysis in a large Swedish family supports the presence of a susceptibility locus for adenoma and colorectal cancer on chromosome 9q22.32-31.1.

Skoglund J, Djureinovic T, Zhou XL, Vandrovcova J, Renkonen E, Iselius L, Bisgaard ML, Peltomäki P, Lindblom A.

J Med Genet. 2006 Feb;43(2):e7.

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