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Items: 1 to 20 of 125

1.

Generation of a 3-Mb PAC contig spanning the Miyoshi myopathy/limb-girdle muscular dystrophy (MM/LGMD2B) locus on chromosome 2p13.

Liu J, Wu C, Bossie K, Bejaoui K, Hosler BA, Gingrich JC, Ben Hamida M, Hentati F, Schurr E, de Jong PJ, Brown RH Jr.

Genomics. 1998 Apr 1;49(1):23-9.

PMID:
9570945
2.

Genetic and physical mapping at the limb-girdle muscular dystrophy locus (LGMD2B) on chromosome 2p.

Bashir R, Keers S, Strachan T, Passos-Bueno R, Zatz M, Weissenbach J, Le Paslier D, Meisler M, Bushby K.

Genomics. 1996 Apr 1;33(1):46-52.

PMID:
8617508
3.

[Miyoshi distal muscular dystrophy].

Hirabayashi K.

Nihon Rinsho. 1997 Dec;55(12):3190-4. Review. Japanese.

PMID:
9436434
4.

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
5.

A sequence-ready high-resolution physical map of the best macular dystrophy gene region in 11q12-q13.

Cooper PR, Nowak NJ, Higgins MJ, Simpson SA, Marquardt A, Stoehr H, Weber BH, Gerhard DS, de Jong PJ, Shows TB.

Genomics. 1997 Apr 15;41(2):185-92.

PMID:
9143493
6.

A sequence-ready 840-kb PAC contig spanning the candidate tumor suppressor locus DBC1 on human chromosome 9q32-q33.

Nishiyama H, Hornigold N, Davies AM, Knowles MA.

Genomics. 1999 Aug 1;59(3):335-8.

PMID:
10444335
7.

Molecular cloning of the interleukin-1 gene cluster: construction of an integrated YAC/PAC contig and a partial transcriptional map in the region of chromosome 2q13.

Nothwang HG, Strahm B, Denich D, Kübler M, Schwabe J, Gingrich JC, Jauch A, Cox A, Nicklin MJ, Kurnit DM, Hildebrandt F.

Genomics. 1997 May 1;41(3):370-8.

PMID:
9169134
8.

Mapping of a chromosome 15 region involved in limb girdle muscular dystrophy.

Fougerousse F, Broux O, Richard I, Allamand V, de Souza AP, Bourg N, Brenguier L, Devaud C, Pasturaud P, Roudaut C, et al.

Hum Mol Genet. 1994 Feb;3(2):285-93.

PMID:
8004096
9.

A sequence-ready BAC/PAC contig and partial transcript map of approximately 1.5 Mb in human chromosome 17q25 comprising multiple disease genes.

Kuhlenbäumer G, Schirmacher A, Meuleman J, Tissir F, Del-Favero J, Stögbauer F, Young P, Ringelstein B, Van Broeckhoven C, Timmerman V.

Genomics. 1999 Dec 1;62(2):242-50.

PMID:
10610718
10.

Construction of a 1-Mb restriction-mapped cosmid contig containing the candidate region for the familial Mediterranean fever locus (MEFV) on chromosome 16p 13.3.

Sood R, Blake T, Aksentijevich I, Wood G, Chen X, Gardner D, Shelton DA, Mangelsdorf M, Orsborn A, Pras E, Balow JE Jr, Centola M, Deng Z, Zaks N, Chen X, Richards N, Fischel-Ghodsian N, Rotter JI, Pras M, Shohat M, Deaven LL, Gumucio DL, Callen DF, Richards RI, Doggett NA, et al.

Genomics. 1997 May 15;42(1):83-95.

PMID:
9177779
11.

YAC contigs of the Rab1 and wobbler (wr) spinal muscular atrophy gene region on proximal mouse chromosome 11 and of the homologous region on human chromosome 2p.

Wedemeyer N, Lengeling A, Ronsiek M, Korthaus D, Baer K, Wuttke M, Jockusch H.

Genomics. 1996 Mar 15;32(3):447-54.

PMID:
8838809
12.

[Mapping of the gene for autosomal-recessive progressive muscular dystrophy in an isolate from a highland region of Dagestan to chromosome 2-13].

Illarioshkin SN, Ivanova-Smolenskaia IA, Dimborskaia SA, Poleshchuk VV, Markova ED, Slominskiĭ PA, Bulaeva KB, Tsudzi Sh.

Genetika. 1997 Nov;33(11):1551-8. Russian.

PMID:
9480219
13.

Clustered cadherin genes: a sequence-ready contig for the desmosomal cadherin locus on human chromosome 18.

Hunt DM, Sahota VK, Taylor K, Simrak D, Hornigold N, Arnemann J, Wolfe J, Buxton RS.

Genomics. 1999 Dec 15;62(3):445-55.

PMID:
10644442
14.

Confirmation of the 2p locus for the mild autosomal recessive limb-girdle muscular dystrophy gene (LGMD2B) in three families allows refinement of the candidate region.

Passos-Bueno MR, Bashir R, Moreira ES, Vainzof M, Marie SK, Vasquez L, Iughetti P, Bakker E, Keers S, Stephenson A, et al.

Genomics. 1995 May 1;27(1):192-5.

PMID:
7665169
15.

A 2.8-Mb clone contig of the multiple endocrine neoplasia type 1 (MEN1) region at 11q13.

Guru SC, Olufemi SE, Manickam P, Cummings C, Gieser LM, Pike BL, Bittner ML, Jiang Y, Chinault AC, Nowak NJ, Brzozowska A, Crabtree JS, Wang Y, Roe BA, Weisemann JM, Boguski MS, Agarwal SK, Burns AL, Spiegel AM, Marx SJ, Flejter WL, de Jong PJ, Collins FS, Chandrasekharappa SC.

Genomics. 1997 Jun 15;42(3):436-45.

PMID:
9205115
16.

Limb-girdle muscular dystrophy and Miyoshi myopathy in an aboriginal Canadian kindred map to LGMD2B and segregate with the same haplotype.

Weiler T, Greenberg CR, Nylen E, Halliday W, Morgan K, Eggertson D, Wrogemann K.

Am J Hum Genet. 1996 Oct;59(4):872-8.

17.

A 1.2-megabase BAC/PAC contig spanning the 14q13 breakpoint of t(2; 14) in a mirror-image polydactyly patient.

Matsumoto N, Soeda E, Ohashi H, Fujimoto M, Kato R, Tsujita T, Tomita H, Kondo S, Fukushima Y, Niikawa N.

Genomics. 1997 Oct 1;45(1):11-6.

PMID:
9339355
18.

A radiation hybrid breakpoint map of the acute myeloid leukemia (AML) and limb-girdle muscular dystrophy 1A (LGMD1A) regions of chromosome 5q31 localizing 122 expressed sequences.

Horrigan SK, Bartoloni L, Speer MC, Fulton N, Kravarusic J, Ramesar R, Vance JM, Yamaoka LH, Westbrook CA.

Genomics. 1999 Apr 1;57(1):24-35.

PMID:
10191080
19.

A 6-Mb high-resolution physical and transcription map encompassing the hereditary prostate cancer 1 (HPC1) region.

Carpten JD, Makalowska I, Robbins CM, Scott N, Sood R, Connors TD, Bonner TI, Smith JR, Faruque MU, Stephan DA, Pinkett H, Morgenbesser SD, Su K, Graham C, Gregory SG, Williams H, McDonald L, Baxevanis AD, Klingler KW, Landes GM, Trent JM.

Genomics. 2000 Feb 15;64(1):1-14.

PMID:
10708513
20.

A 1.5-Mb physical map of the hidrotic ectodermal dysplasia (Clouston syndrome) gene region on human chromosome 13q11.

Lamartine J, Pitaval A, Soularue P, Lanneluc I, Lemaître G, Kibar Z, Rouleau GA, Waksman G.

Genomics. 2000 Jul 15;67(2):232-6.

PMID:
10903849

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