Strachan T - Search Results

1

Bashir R, Britton S, Strachan T, Keers S, Vafiadaki E, Lako M, Richard I, Marchand S, Bourg N, Argov Z, Sadeh M, Mahjneh I, Marconi G, Passos-Bueno MR, Moreira Ede S, Zatz M, Beckmann JS, Bushby K. Bashir R, et al. Among authors: strachan t. Nat Genet. 1998 Sep;20(1):37-42. doi: 10.1038/1689. Nat Genet. 1998. PMID: 9731527

2

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, Bushby KM. Bashir R, et al. Among authors: strachan t. Hum Mol Genet. 1994 Mar;3(3):455-7. doi: 10.1093/hmg/3.3.455. Hum Mol Genet. 1994. PMID: 8012357

3

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. Bashir R, et al. Among authors: strachan t. Genomics. 1996 Apr 1;33(1):46-52. doi: 10.1006/geno.1996.0157. Genomics. 1996. PMID: 8617508

4

The molecular biology of LGMD2B--towards the identification of the LGMD gene on chromosome 2p13.

Bushby K, Bashir R, Keers S, Britton S, Zatz M, Passos-Bueno MR, Lovett M, Mahjneh I, Marconi G, Strachan T. Bushby K, et al. Among authors: strachan t. Neuromuscul Disord. 1996 Dec;6(6):491-2. doi: 10.1016/s0960-8966(96)00393-8. Neuromuscul Disord. 1996. PMID: 9027860 No abstract available.

5

Isolation and characterization of WNT8B, a novel human Wnt gene that maps to 10q24.

Lako M, Strachan T, Curtis AR, Lindsay S. Lako M, et al. Among authors: strachan t. Genomics. 1996 Jul 15;35(2):386-8. doi: 10.1006/geno.1996.0374. Genomics. 1996. PMID: 8661156

6

Main clinical features of the three mapped autosomal recessive limb-girdle muscular dystrophies and estimated proportion of each form in 13 Brazilian families.

Passos-Bueno MR, Moreira ES, Marie SK, Bashir R, Vasquez L, Love DR, Vainzof M, Iughetti P, Oliveira JR, Bakker E, Strachan T, Bushby K, Zatz M. Passos-Bueno MR, et al. Among authors: strachan t. J Med Genet. 1996 Feb;33(2):97-102. doi: 10.1136/jmg.33.2.97. J Med Genet. 1996. PMID: 8929943 Free PMC article.

7

A new dimension for the human genome project: towards comprehensive expression maps.

Strachan T, Abitbol M, Davidson D, Beckmann JS. Strachan T, et al. Nat Genet. 1997 Jun;16(2):126-32. doi: 10.1038/ng0697-126. Nat Genet. 1997. PMID: 9171823 Review.

8

Mutation screening in British 21-hydroxylase deficiency families and development of novel microsatellite based approaches to prenatal diagnosis.

Lako M, Ramsden S, Campbell RD, Strachan T. Lako M, et al. Among authors: strachan t. J Med Genet. 1999 Feb;36(2):119-24. J Med Genet. 1999. PMID: 10051010 Free PMC article.

9

Partial cloning and assignment of WNT6 to human chromosome band 2q35 by in situ hybridization.

Rankin J, Strachan T, Lako M, Lindsay S. Rankin J, et al. Among authors: strachan t. Cytogenet Cell Genet. 1999;84(1-2):50-2. doi: 10.1159/000015212. Cytogenet Cell Genet. 1999. PMID: 10343101 No abstract available.

10

Localisation of a gene for Darier's disease.

Bashir R, Munro CS, Mason S, Stephenson A, Rees JL, Strachan T. Bashir R, et al. Among authors: strachan t. Hum Mol Genet. 1993 Nov;2(11):1937-9. doi: 10.1093/hmg/2.11.1937. Hum Mol Genet. 1993. PMID: 7506604 No abstract available.

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