SCOPUS 정보 검색 플랫폼

Volumn 59, Issue 4, 1996, Pages 872-878

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

(7) Weiler, Tracey b Greenberg, Cheryl R b Nylen, Edward b Halliday, William b Morgan, Kenneth b Eggertson, Douglas b Wrogemann, Klaus a

a UNIVERSITY OF MANITOBA (Canada)

b NONE

Author keywords

[No Author keywords available]

Indexed keywords

ABORIGINE; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CANADA; CLINICAL ARTICLE; DNA DETERMINATION; FEMALE; GENE MAPPING; GENE MUTATION; GENE SEGREGATION; GENETIC LINKAGE; HAPLOTYPE; HUMAN; INBREEDING; LIMB GIRDLE MUSCULAR DYSTROPHY; MALE; MYOPATHY; PEDIGREE; PRIORITY JOURNAL;

ADOLESCENT; ADULT; AGE OF ONSET; AMERICAN NATIVE CONTINENTAL ANCESTRY GROUP; CANADA; CHROMOSOMES, HUMAN, PAIR 2; FEMALE; HAPLOIDY; HUMANS; LINKAGE (GENETICS); MALE; MICROSATELLITE REPEATS; MUSCULAR DYSTROPHIES; PEDIGREE;

EID: 0029845713 PISSN: 00029297 EISSN: None Source Type: Journal
DOI: None Document Type: Article

Times cited : (91)

References (5)

1
- 0028997311
- Preferential localization of the limb-girdle muscular dystrophy type 2A gene in the proximal part of a 1-cM 15ql5.1-ql5.3 interval
- Allamand V, Broux O, Richard I, Fougerousse F, Chiannilkulchai N, Bourg N, Brenguier L, et al (1995) Preferential localization of the limb-girdle muscular dystrophy type 2A gene in the proximal part of a 1-cM 15ql5.1-ql5.3 interval. Am J Hum Genet 56:1417-1430
- (1995) Am J Hum Genet , vol.56 , pp. 1417-1430
- Allamand, V.¹ Broux, O.² Richard, I.³ Fougerousse, F.⁴ Chiannilkulchai, N.⁵ Bourg, N.⁶ Brenguier, L.⁷

2
- 0028326542
- A gene for autosomal recessive limb-girdle muscular dystrophy maps to chromosome 2p
- Bashir R, Strachan T, Keers S, Stephenson A, Mahjneh I, Marconi G, Nashef L, et al (1994) A gene for autosomal recessive limb-girdle muscular dystrophy maps to chromosome 2p. Hum Mol Genet 3:455-457
- (1994) Hum Mol Genet , vol.3 , pp. 455-457
- Bashir, R.¹ Strachan, T.² Keers, S.³ Stephenson, A.⁴ Mahjneh, I.⁵ Marconi, G.⁶ Nashef, L.⁷

3
- 0028951204
- Linkage of Miyoshi myopathy (distal autosomal recessive muscular dystrophy) locus to chromosome 2p12-14
- Bejaoui K, Hirabayashi K, Hentati F, Haines JL, Ben-Hamida C, Belal S, Miller RG, et al (1995) Linkage of Miyoshi myopathy (distal autosomal recessive muscular dystrophy) locus to chromosome 2p12-14. Neurology 45:768-772
- (1995) Neurology , vol.45 , pp. 768-772
- Bejaoui, K.¹ Hirabayashi, K.² Hentati, F.³ Haines, J.L.⁴ Ben-Hamida, C.⁵ Belal, S.⁶ Miller, R.G.⁷

4
- 0027032694
- Linkage of Tunisian autosomal recessive Duchenne-like muscular dystrophy to the pericentromeric region of chromosome 13q
- Ben-Othmane K, Ben-Hamida M, Pericak-Vance MA, Ben-Hamida C, Blel S, Carter SC, Bowcock AM, et al (1992) Linkage of Tunisian autosomal recessive Duchenne-like muscular dystrophy to the pericentromeric region of chromosome 13q. Nat Genet 2:315-317
- (1992) Nat Genet , vol.2 , pp. 315-317
- Ben-Othmane, K.¹ Ben-Hamida, M.² Ma, P.-V.³ Ben-Hamida, C.⁴ Blel, S.⁵ Carter, S.C.⁶ Bowcock, A.M.⁷

5
- 0029152259
- Evidence for linkage disequilibrium in chromosome 13-linked Duchenne-like muscular dystrophy (LGMD2C)
- Ben Othmane K, Speer MC, Stauffer J, Blel S, Middleton L, Ben Hamida C, Etribi A, et al (1995) Evidence for linkage disequilibrium in chromosome 13-linked Duchenne-like muscular dystrophy (LGMD2C). Am J Hum Genet 57:732-734
- (1995) Am J Hum Genet , vol.57 , pp. 732-734
- Ben Othmane, K.¹ Speer, M.C.² Stauffer, J.³ Blel, S.⁴ Middleton, L.⁵ Ben Hamida, C.⁶ Etribi, A.⁷

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.