Buckle VJ - Search Results

1

The identification of a third fragile site, FRAXF, in Xq27--q28 distal to both FRAXA and FRAXE.

Hirst MC, Barnicoat A, Flynn G, Wang Q, Daker M, Buckle VJ, Davies KE, Bobrow M. Hirst MC, et al. Among authors: buckle vj. Hum Mol Genet. 1993 Feb;2(2):197-200. doi: 10.1093/hmg/2.2.197. Hum Mol Genet. 1993. PMID: 8499907

2

X-linked alpha-thalassemia/mental retardation (ATR-X) syndrome: localization to Xq12-q21.31 by X inactivation and linkage analysis.

Gibbons RJ, Suthers GK, Wilkie AO, Buckle VJ, Higgs DR. Gibbons RJ, et al. Among authors: buckle vj. Am J Hum Genet. 1992 Nov;51(5):1136-49. Am J Hum Genet. 1992. PMID: 1415255 Free PMC article.

3

High-resolution genetic map around the spinal muscular atrophy (SMA) locus on chromosome 5.

Morrison KE, Daniels RJ, Suthers GK, Flynn GA, Francis MJ, Buckle VJ, Davies KE. Morrison KE, et al. Among authors: buckle vj. Am J Hum Genet. 1992 Mar;50(3):520-7. Am J Hum Genet. 1992. PMID: 1539593 Free PMC article.

4

Localisation of a dystrophin-related autosomal gene to 6q24 in man, and to mouse chromosome 10 in the region of the dystrophia muscularis (dy) locus.

Buckle VJ, Guenet JL, Simon-Chazottes D, Love DR, Davies KE. Buckle VJ, et al. Hum Genet. 1990 Aug;85(3):324-6. doi: 10.1007/BF00206755. Hum Genet. 1990. PMID: 2203673

5

Clinical features and molecular analysis of the alpha thalassemia/mental retardation syndromes. I. Cases due to deletions involving chromosome band 16p13.3.

Wilkie AO, Buckle VJ, Harris PC, Lamb J, Barton NJ, Reeders ST, Lindenbaum RH, Nicholls RD, Barrow M, Bethlenfalvay NC, et al. Wilkie AO, et al. Among authors: buckle vj. Am J Hum Genet. 1990 Jun;46(6):1112-26. Am J Hum Genet. 1990. PMID: 2339704 Free PMC article.

6

Clinical features and molecular analysis of the alpha thalassemia/mental retardation syndromes. II. Cases without detectable abnormality of the alpha globin complex.

Wilkie AO, Zeitlin HC, Lindenbaum RH, Buckle VJ, Fischel-Ghodsian N, Chui DH, Gardner-Medwin D, MacGillivray MH, Weatherall DJ, Higgs DR. Wilkie AO, et al. Among authors: buckle vj. Am J Hum Genet. 1990 Jun;46(6):1127-40. Am J Hum Genet. 1990. PMID: 2339705 Free PMC article.

7

Clinical and hematologic aspects of the X-linked alpha-thalassemia/mental retardation syndrome (ATR-X).

Gibbons RJ, Brueton L, Buckle VJ, Burn J, Clayton-Smith J, Davison BC, Gardner RJ, Homfray T, Kearney L, Kingston HM, et al. Gibbons RJ, et al. Among authors: buckle vj. Am J Med Genet. 1995 Jan 30;55(3):288-99. doi: 10.1002/ajmg.1320550309. Am J Med Genet. 1995. PMID: 7726225 Review.

8

Dissecting the centromere of the human Y chromosome with cloned telomeric DNA.

Brown KE, Barnett MA, Burgtorf C, Shaw P, Buckle VJ, Brown WR. Brown KE, et al. Among authors: buckle vj. Hum Mol Genet. 1994 Aug;3(8):1227-37. doi: 10.1093/hmg/3.8.1227. Hum Mol Genet. 1994. PMID: 7987296

9

Characterisation of molecular DNA rearrangements within the Xq12-q13.1 region, in three patients with X-linked hypohidrotic ectodermal dysplasia (EDA).

Thomas NS, Chelly J, Zonana J, Davies KJ, Morgan S, Gault J, Rack KA, Buckle VJ, Brockdorff N, Clarke A, et al. Thomas NS, et al. Among authors: buckle vj. Hum Mol Genet. 1993 Oct;2(10):1679-85. doi: 10.1093/hmg/2.10.1679. Hum Mol Genet. 1993. PMID: 8268921

10

Two novel microsatellite markers for prenatal prediction of spinal muscular atrophy (SMA).

Morrison KE, Daniels RJ, Suthers GK, Flynn GA, Francis MJ, Grewal PK, Dennis C, Buckle V, Ignatius J, Dubowitz V, et al. Morrison KE, et al. Hum Genet. 1993 Sep;92(2):133-8. doi: 10.1007/BF00219680. Hum Genet. 1993. PMID: 8370578

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

106 results

Search Page

Filters