Daniels R - Search Results

1

Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q11.2-13.3.

Brzustowicz LM, Lehner T, Castilla LH, Penchaszadeh GK, Wilhelmsen KC, Daniels R, Davies KE, Leppert M, Ziter F, Wood D, et al. Brzustowicz LM, et al. Among authors: daniels r. Nature. 1990 Apr 5;344(6266):540-1. doi: 10.1038/344540a0. Nature. 1990. PMID: 2320125

2

Genetic homogeneity between acute and chronic forms of spinal muscular atrophy.

Gilliam TC, Brzustowicz LM, Castilla LH, Lehner T, Penchaszadeh GK, Daniels RJ, Byth BC, Knowles J, Hislop JE, Shapira Y, et al. Gilliam TC, et al. Among authors: daniels rj. Nature. 1990 Jun 28;345(6278):823-5. doi: 10.1038/345823a0. Nature. 1990. PMID: 1972783

3

An investigation of genetic heterogeneity and linkage disequilibrium in 161 families with spinal muscular atrophy.

Mérette C, Brzustowicz LM, Daniels RJ, Davies KE, Gilliam TC, Melki J, Munnich A, Pericak-Vance MA, Siddique T, Voosen B, et al. Mérette C, et al. Among authors: daniels rj. Genomics. 1994 May 1;21(1):27-33. doi: 10.1006/geno.1994.1220. Genomics. 1994. PMID: 8088801 Free article.

4

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.

5

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.

6

Spinal muscular atrophy in trizygotic triplets.

Komatsu H, Takeuchi Y, Miyanomae Y, Yoshioka H, Daniels R, Davies KE, Sawada T. Komatsu H, et al. Among authors: daniels r. Acta Paediatr Jpn. 1994 Oct;36(5):522-6. doi: 10.1111/j.1442-200x.1994.tb03239.x. Acta Paediatr Jpn. 1994. PMID: 7825456

7

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

8

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.

9

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.

10

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.

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