Jackson CE - Search Results

1

Confirmation of linkage of limb-girdle muscular dystrophy, type 2, to chromosome 15.

Young K, Foroud T, Williams P, Jackson CE, Beckmann JS, Cohen D, Conneally PM, Tischfield J, Hodes ME. Young K, et al. Among authors: jackson ce. Genomics. 1992 Aug;13(4):1370-1. doi: 10.1016/0888-7543(92)90074-3. Genomics. 1992. PMID: 1505977 No abstract available.

2

Genetic heterogeneity of autosomal recessive limb-girdle muscular dystrophy in a genetic isolate (Amish) and evidence for a new locus.

Allamand V, Broux O, Bourg N, Richard I, Tischfield JA, Hodes ME, Conneally PM, Fardeau M, Jackson CE, Beckmann JS. Allamand V, et al. Among authors: jackson ce. Hum Mol Genet. 1995 Mar;4(3):459-63. doi: 10.1093/hmg/4.3.459. Hum Mol Genet. 1995. PMID: 7795603

3

Limb-girdle muscular dystrophy is closely linked to the fibrillin locus on chromosome 15.

Velinov M, Sarfarazi M, Young K, Hodes ME, Conneally PM, Jackson CE, Tsipouras P. Velinov M, et al. Among authors: jackson ce. Connect Tissue Res. 1993;29(1):13-21. doi: 10.3109/03008209309061962. Connect Tissue Res. 1993. PMID: 8339542

4

Possible linear order of genes for endocrine neoplasia type 2, the P red cell antigen and HL-A on chromosome 6.

Jackson CE, Conneally PM, Sizemore GW, Tashjian AH. Jackson CE, et al. Birth Defects Orig Artic Ser. 1976;12(1):159-64. Birth Defects Orig Artic Ser. 1976. PMID: 990440 No abstract available.

5

Multiple independent molecular etiology for limb-girdle muscular dystrophy type 2A patients from various geographical origins.

Richard I, Brenguier L, Dinçer P, Roudaut C, Bady B, Burgunder JM, Chemaly R, Garcia CA, Halaby G, Jackson CE, Kurnit DM, Lefranc G, Legum C, Loiselet J, Merlini L, Nivelon-Chevallier A, Ollagnon-Roman E, Restagno G, Topaloglu H, Beckmann JS. Richard I, et al. Among authors: jackson ce. Am J Hum Genet. 1997 May;60(5):1128-38. Am J Hum Genet. 1997. PMID: 9150160 Free PMC article.

6

A diagnostic fluorescent marker kit for six limb girdle muscular dystrophies.

Richard I, Bourg N, Marchand S, Alibert O, Eymard B, van der Kooi AJ, Jackson CE, Garcia C, Burgunder JM, Legum C, de Visser M, Fardeau M, Beckmann JS. Richard I, et al. Among authors: jackson ce. Neuromuscul Disord. 1999 Dec;9(8):555-63. doi: 10.1016/s0960-8966(99)00037-1. Neuromuscul Disord. 1999. PMID: 10619713

7

Identification of muscle-specific calpain and beta-sarcoglycan genes in progressive autosomal recessive muscular dystrophies.

Beckmann JS, Richard I, Broux O, Fougerousse F, Allamand V, Chiannilkulchai N, Lim LE, Duclos F, Bourg N, Brenguier L, Pasturaud P, Quétier F, Roudaut C, Sunada Y, Meyer J, Dinçer P, Lefranc G, Merlini L, Topaloglu H, Tomé FM, Cohen D, Jackson CE, Campbell KP, Fardeau M. Beckmann JS, et al. Among authors: jackson ce. Neuromuscul Disord. 1996 Dec;6(6):455-62. doi: 10.1016/s0960-8966(96)00386-0. Neuromuscul Disord. 1996. PMID: 9027855

8

Linkage relations of the loci for Kell and phenylthiocarbamide taste sensitivity.

Conneally PM, Dumont-Driscoll M, Huntzinger RS, Nance WE, Jackson CE. Conneally PM, et al. Among authors: jackson ce. Hum Hered. 1976;26(4):267-71. doi: 10.1159/000152813. Hum Hered. 1976. PMID: 976995

9

Vocal cord and pharyngeal weakness with autosomal dominant distal myopathy: clinical description and gene localization to 5q31.

Feit H, Silbergleit A, Schneider LB, Gutierrez JA, Fitoussi RP, Réyès C, Rouleau GA, Brais B, Jackson CE, Beckmann JS, Seboun E. Feit H, et al. Among authors: jackson ce. Am J Hum Genet. 1998 Dec;63(6):1732-42. doi: 10.1086/302166. Am J Hum Genet. 1998. PMID: 9837826 Free PMC article.

10

Beta-sarcoglycan: genomic analysis and identification of a novel missense mutation in the LGMD2E Amish isolate.

Duclos F, Broux O, Bourg N, Straub V, Feldman GL, Sunada Y, Lim LE, Piccolo F, Cutshall S, Gary F, Quetier F, Kaplan JC, Jackson CE, Beckmann JS, Campbell KP. Duclos F, et al. Among authors: jackson ce. Neuromuscul Disord. 1998 Feb;8(1):30-8. doi: 10.1016/s0960-8966(97)00135-1. Neuromuscul Disord. 1998. PMID: 9565988

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