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Results: 1 to 20 of 196

Related Citations for PubMed (Select 10407851)

1.

A second locus for autosomal dominant myopathy with proximal muscle weakness and early respiratory muscle involvement: a likely chromosomal locus on 2q21.

Xiang F, Nicolao P, Chapon F, Edström L, Anvret M, Zhang Z.

Neuromuscul Disord. 1999 Jul;9(5):308-12.

PMID:
10407851
2.

Autosomal dominant myopathy with proximal weakness and early respiratory muscle involvement maps to chromosome 2q.

Nicolao P, Xiang F, Gunnarsson LG, Giometto B, Edström L, Anvret M, Zhang Z.

Am J Hum Genet. 1999 Mar;64(3):788-92.

3.

Genetic linkage of Welander distal myopathy to chromosome 2p13.

Ahlberg G, von Tell D, Borg K, Edström L, Anvret M.

Ann Neurol. 1999 Sep;46(3):399-404.

PMID:
10482271
4.

Vocal cord and pharyngeal weakness with autosomal dominant distal myopathy: clinical description and gene localization to 5q31.

Feit H, Silbergleit A, Schneider LB, Gutierrez JA, Fitoussi RP, Réyès C, Rouleau GA, Brais B, Jackson CE, Beckmann JS, Seboun E.

Am J Hum Genet. 1998 Dec;63(6):1732-42.

5.

Gene locus for autosomal recessive distal myopathy with rimmed vacuoles maps to chromosome 9.

Ikeuchi T, Asaka T, Saito M, Tanaka H, Higuchi S, Tanaka K, Saida K, Uyama E, Mizusawa H, Fukuhara N, Nonaka I, Takamori M, Tsuji S.

Ann Neurol. 1997 Apr;41(4):432-7.

PMID:
9124799
6.

Assignment of the tibial muscular dystrophy locus to chromosome 2q31.

Haravuori H, Mäkelä-Bengs P, Udd B, Partanen J, Pulkkinen L, Somer H, Peltonen L.

Am J Hum Genet. 1998 Mar;62(3):620-6.

7.

A genome-wide scan maps a novel autosomal dominant juvenile-onset open-angle glaucoma locus to 2p15-16.

Lin Y, Liu T, Li J, Yang J, Du Q, Wang J, Yang Y, Liu X, Fan Y, Lu F, Chen Y, Pu Y, Zhang K, He X, Yang Z.

Mol Vis. 2008 Apr 18;14:739-44.

8.

A new locus for autosomal dominant pure spastic paraplegia, on chromosome 2q24-q34.

Fontaine B, Davoine CS, Dürr A, Paternotte C, Feki I, Weissenbach J, Hazan J, Brice A.

Am J Hum Genet. 2000 Feb;66(2):702-7.

9.

Dominant hereditary inclusion-body myopathy gene (IBM3) maps to chromosome region 17p13.1.

Martinsson T, Darin N, Kyllerman M, Oldfors A, Hallberg B, Wahlström J.

Am J Hum Genet. 1999 May;64(5):1420-6.

10.

Linkage of X-linked myopathy with excessive autophagy (XMEA) to Xq28.

Villard L, des Portes V, Levy N, Louboutin JP, Recan D, Coquet M, Chabrol B, Figarella-Branger D, Chelly J, Pellissier JF, Fontes M.

Eur J Hum Genet. 2000 Feb;8(2):125-9.

11.

Autosomal dominant distal myopathy: linkage to chromosome 14.

Laing NG, Laing BA, Meredith C, Wilton SD, Robbins P, Honeyman K, Dorosz S, Kozman H, Mastaglia FL, Kakulas BA.

Am J Hum Genet. 1995 Feb;56(2):422-7.

12.

Autosomal dominant distal myopathy: further evidence of a chromosome 14 locus.

Voit T, Kutz P, Leube B, Neuen-Jacob E, Schröder JM, Cavallotti D, Vaccario ML, Schaper J, Broich P, Cohn R, Baethmann M, Göhlich-Ratmann G, Scoppetta C, Herrmann R.

Neuromuscul Disord. 2001 Jan;11(1):11-9.

PMID:
11166161
13.

Autosomal dominant distal myopathy not linked to the known distal myopathy loci.

Felice KJ, Meredith C, Binz N, Butler A, Jacob R, Akkari P, Hallmayer J, Laing N.

Neuromuscul Disord. 1999 Mar;9(2):59-65.

PMID:
10220859
14.

A gene for autosomal recessive limb-girdle muscular dystrophy in Manitoba Hutterites maps to chromosome region 9q31-q33: evidence for another limb-girdle muscular dystrophy locus.

Weiler T, Greenberg CR, Zelinski T, Nylen E, Coghlan G, Crumley MJ, Fujiwara TM, Morgan K, Wrogemann K.

Am J Hum Genet. 1998 Jul;63(1):140-7.

15.

Linkage to two separate loci in a family with a novel distal myopathy phenotype (MPD3).

Haravuori H, Siitonen HA, Mahjneh I, Hackman P, Lahti L, Somer H, Peltonen L, Kestilä M, Udd B.

Neuromuscul Disord. 2004 Mar;14(3):183-7.

PMID:
15036327
16.

Clinical delineation and localization to chromosome 9p13.3-p12 of a unique dominant disorder in four families: hereditary inclusion body myopathy, Paget disease of bone, and frontotemporal dementia.

Kovach MJ, Waggoner B, Leal SM, Gelber D, Khardori R, Levenstien MA, Shanks CA, Gregg G, Al-Lozi MT, Miller T, Rakowicz W, Lopate G, Florence J, Glosser G, Simmons Z, Morris JC, Whyte MP, Pestronk A, Kimonis VE.

Mol Genet Metab. 2001 Dec;74(4):458-75.

PMID:
11749051
17.

Genetic fine mapping of the Miyoshi myopathy locus and exclusion of eight candidate genes.

Bejaoui K, Liu J, McKenna-Yasek D, Le Paslier D, Bossie K, Gilligan DM, Brown RH.

Neurogenetics. 1998 Mar;1(3):189-96.

PMID:
10737122
18.

Refined genetic location of the chromosome 2p-linked progressive muscular dystrophy gene.

Illarioshkin SN, Ivanova-Smolenskaya IA, Tanaka H, Poleshchuk VV, Markova ED, Tsuji S.

Genomics. 1997 Jun 1;42(2):345-8.

PMID:
9192858
19.

A locus on chromosome 15q for a dominantly inherited nemaline myopathy with core-like lesions.

Gommans IM, Davis M, Saar K, Lammens M, Mastaglia F, Lamont P, van Duijnhoven G, ter Laak HJ, Reis A, Vogels OJ, Laing N, van Engelen BG, Kremer H.

Brain. 2003 Jul;126(Pt 7):1545-51. Epub 2003 Jun 4. Erratum in: Brain. 2003 Sep;126(Pt 9):2115.

20.

Autosomal dominant progressive nephropathy with deafness: linkage to a new locus on chromosome 11q24.

Prakash S, Chung KW, Sinha S, Barmada M, Ellis D, Ferrell RE, Finegold DN, Randhawa PS, Dinda A, Vats A.

J Am Soc Nephrol. 2003 Jul;14(7):1794-803.

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