Storvick D[au] - Search Results

Year	Number of Results
1992	3
1993	4
2023	0

1

Linkage of atypical myotonia congenita to a sodium channel locus.

Ptacek LJ, Tawil R, Griggs RC, Storvick D, Leppert M. Ptacek LJ, et al. Among authors: storvick d. Neurology. 1992 Feb;42(2):431-3. doi: 10.1212/wnl.42.2.431. Neurology. 1992. PMID: 1310531

2

Chromosome 4q DNA rearrangement in monozygotic twins discordant for facioscapulohumeral muscular dystrophy.

Tawil R, Storvick D, Weiffenbach B, Altherr MR, Feasby TE, Griggs RC. Tawil R, et al. Among authors: storvick d. Hum Mutat. 1993;2(6):492-4. doi: 10.1002/humu.1380020612. Hum Mutat. 1993. PMID: 8111417 No abstract available.

3

Mapping the facioscapulohumeral muscular dystrophy gene is complicated by chromsome 4q35 recombination events.

Weiffenbach B, Dubois J, Storvick D, Tawil R, Jacobsen SJ, Gilbert J, Wijmenga C, Mendell JR, Winokur S, Altherr MR, et al. Weiffenbach B, et al. Among authors: storvick d. Nat Genet. 1993 Jun;4(2):165-9. doi: 10.1038/ng0693-165. Nat Genet. 1993. PMID: 8102297

4

Extreme variability of expression in monozygotic twins with FSH muscular dystrophy.

Tawil R, Storvick D, Feasby TE, Weiffenbach B, Griggs RC. Tawil R, et al. Among authors: storvick d. Neurology. 1993 Feb;43(2):345-8. doi: 10.1212/wnl.43.2.345. Neurology. 1993. PMID: 8094896

5

Framework multipoint map of the long arm of human chromosome 4 and telomeric localization of the gene for FSHD.

Weiffenbach B, Bagley RG, Falls K, Dubois J, Hyser C, Storvick D, Schultz P, Mendell JR, Milner EC, Jacobsen SJ, et al. Weiffenbach B, et al. Among authors: storvick d. Mamm Genome. 1992;3(3):143-50. doi: 10.1007/BF00352458. Mamm Genome. 1992. PMID: 1352159

6

Linkage analyses of five chromosome 4 markers localizes the facioscapulohumeral muscular dystrophy (FSHD) gene to distal 4q35.

Weiffenbach B, Bagley R, Falls K, Hyser C, Storvick D, Jacobsen SJ, Schultz P, Mendell J, Willems van Dijk K, Milner EC, et al. Weiffenbach B, et al. Among authors: storvick d. Am J Hum Genet. 1992 Aug;51(2):416-23. Am J Hum Genet. 1992. PMID: 1642240 Free PMC article.

7

Genetics of facioscapulohumeral muscular dystrophy: new mutations in sporadic cases.

Griggs RC, Tawil R, Storvick D, Mendell JR, Altherr MR. Griggs RC, et al. Among authors: storvick d. Neurology. 1993 Nov;43(11):2369-72. doi: 10.1212/wnl.43.11.2369. Neurology. 1993. PMID: 8232958

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