Campbell L - Search Results

1

Genomic rearrangements in childhood spinal muscular atrophy: linkage disequilibrium with a null allele.

Daniels RJ, Campbell L, Rodrigues NR, Francis MJ, Morrison KE, McLean M, MacKenzie A, Ignatius J, Dubowitz V, Davies KE. Daniels RJ, et al. Among authors: campbell l. J Med Genet. 1995 Feb;32(2):93-6. doi: 10.1136/jmg.32.2.93. J Med Genet. 1995. PMID: 7760328 Free PMC article.

2

Mapping of retrotransposon sequences in the unstable region surrounding the spinal muscular atrophy locus in 5q13.

Francis MJ, Nesbit MA, Theodosiou AM, Rodrigues NR, Campbell L, Christodoulou Z, Qureshi SJ, Porteous DJ, Brookes AJ, Davies KE. Francis MJ, et al. Among authors: campbell l. Genomics. 1995 May 20;27(2):366-9. doi: 10.1006/geno.1995.1059. Genomics. 1995. PMID: 7558009

3

Dinucleotide repeat polymorphism proximal to the spinal muscular atrophy region at D5S681.

Morrison KE, Daniels RJ, Campbell L, McPherson J, Davies KE. Morrison KE, et al. Among authors: campbell l. Hum Mol Genet. 1993 Oct;2(10):1753. doi: 10.1093/hmg/2.10.1753. Hum Mol Genet. 1993. PMID: 8268953 No abstract available.

4

A contig of non-chimaeric YACs containing the spinal muscular atrophy gene in 5q13.

Francis MJ, Morrison KE, Campbell L, Grewal PK, Christodoulou Z, Daniels RJ, Monaco AP, Frischauf AM, McPherson J, Wasmuth J, et al. Francis MJ, et al. Among authors: campbell l. Hum Mol Genet. 1993 Aug;2(8):1161-7. doi: 10.1093/hmg/2.8.1161. Hum Mol Genet. 1993. PMID: 8401497

5

Genomic variation and gene conversion in spinal muscular atrophy: implications for disease process and clinical phenotype.

Campbell L, Potter A, Ignatius J, Dubowitz V, Davies K. Campbell L, et al. Am J Hum Genet. 1997 Jul;61(1):40-50. doi: 10.1086/513886. Am J Hum Genet. 1997. PMID: 9245983 Free PMC article.

6

Maternal mosaicism for a second mutational event in a type I spinal muscular atrophy family.

Campbell L, Daniels RJ, Dubowitz V, Davies KE. Campbell L, et al. Am J Hum Genet. 1998 Jul;63(1):37-44. doi: 10.1086/301918. Am J Hum Genet. 1998. PMID: 9634516 Free PMC article.

7

Prenatal diagnosis of spinal muscular atrophy by gene deletion analysis.

Rodrigues NR, Campbell L, Owen N, Rodeck CH, Davies KE. Rodrigues NR, et al. Among authors: campbell l. Lancet. 1995 Apr 22;345(8956):1049. doi: 10.1016/s0140-6736(95)90787-4. Lancet. 1995. PMID: 7723516 No abstract available.

8

Complex repetitive arrangements of gene sequence in the candidate region of the spinal muscular atrophy gene in 5q13.

Theodosiou AM, Morrison KE, Nesbit AM, Daniels RJ, Campbell L, Francis MJ, Christodoulou Z, Davies KE. Theodosiou AM, et al. Among authors: campbell l. Am J Hum Genet. 1994 Dec;55(6):1209-17. Am J Hum Genet. 1994. PMID: 7977382 Free PMC article.

9

The utrophin and dystrophin genes share similarities in genomic structure.

Pearce M, Blake DJ, Tinsley JM, Byth BC, Campbell L, Monaco AP, Davies KE. Pearce M, et al. Among authors: campbell l. Hum Mol Genet. 1993 Nov;2(11):1765-72. doi: 10.1093/hmg/2.11.1765. Hum Mol Genet. 1993. PMID: 8281135

10

Direct interaction of Smn with dp103, a putative RNA helicase: a role for Smn in transcription regulation?

Campbell L, Hunter KM, Mohaghegh P, Tinsley JM, Brasch MA, Davies KE. Campbell L, et al. Hum Mol Genet. 2000 Apr 12;9(7):1093-100. doi: 10.1093/hmg/9.7.1093. Hum Mol Genet. 2000. PMID: 10767334

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