Daniels RJ - Search Results

1

Characterization of deletions in the dystrophin gene giving mild phenotypes.

Love DR, Flint TJ, Marsden RF, Bloomfield JF, Daniels RJ, Forrest SM, Gabrielli O, Giorgi P, Novelli G, Davies KE. Love DR, et al. Among authors: daniels rj. Am J Med Genet. 1990 Sep;37(1):136-42. doi: 10.1002/ajmg.1320370132. Am J Med Genet. 1990. PMID: 2240031

2

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: daniels rj. Am J Hum Genet. 1992 Mar;50(3):520-7. Am J Hum Genet. 1992. PMID: 1539593 Free PMC article.

3

Molecular studies of spinal muscular atrophy.

Davies KE, Thomas NH, Daniels RJ, Dubowitz V. Davies KE, et al. Among authors: daniels rj. Neuromuscul Disord. 1991;1(2):83-5. doi: 10.1016/0960-8966(91)90053-u. Neuromuscul Disord. 1991. PMID: 1822785 Review.

4

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. 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.

5

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. Among authors: daniels rj. Am J Hum Genet. 1998 Jul;63(1):37-44. doi: 10.1086/301918. Am J Hum Genet. 1998. PMID: 9634516 Free PMC article.

6

Linkage analysis of spinal muscular atrophy.

Daniels RJ, Thomas NH, MacKinnon RN, Lehner T, Ott J, Flint TJ, Dubowitz V, Ignatius J, Donner M, Zerres K, et al. Daniels RJ, et al. Genomics. 1992 Feb;12(2):335-9. doi: 10.1016/0888-7543(92)90382-3. Genomics. 1992. PMID: 1346777

7

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: daniels rj. Hum Mol Genet. 1993 Oct;2(10):1753. doi: 10.1093/hmg/2.10.1753. Hum Mol Genet. 1993. PMID: 8268953 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: daniels rj. Am J Hum Genet. 1994 Dec;55(6):1209-17. Am J Hum Genet. 1994. PMID: 7977382 Free PMC article.

9

Olivopontocerebellar hypoplasia with anterior horn cell involvement (SMA) does not localize to chromosome 5q.

Dubowitz V, Daniels RJ, Davies KE. Dubowitz V, et al. Among authors: daniels rj. Neuromuscul Disord. 1995 Jan;5(1):25-9. doi: 10.1016/0960-8966(94)00043-9. Neuromuscul Disord. 1995. PMID: 7719137 No abstract available.

10

Prenatal prediction of spinal muscular atrophy.

Daniels RJ, Suthers GK, Morrison KE, Thomas NH, Francis MJ, Mathew CG, Loughlin S, Heiberg A, Wood D, Dubowitz V, et al. Daniels RJ, et al. J Med Genet. 1992 Mar;29(3):165-70. doi: 10.1136/jmg.29.3.165. J Med Genet. 1992. PMID: 1348091 Free PMC article.

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