Liechti-Gallati S - Search Results

1

An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus.

Monaco AP, Bertelson CJ, Liechti-Gallati S, Moser H, Kunkel LM. Monaco AP, et al. Genomics. 1988 Jan;2(1):90-5. doi: 10.1016/0888-7543(88)90113-9. Genomics. 1988. PMID: 3384440

2

Molecular deletion patterns in Duchenne and Becker type muscular dystrophy.

Liechti-Gallati S, Koenig M, Kunkel LM, Frey D, Boltshauser E, Schneider V, Braga S, Moser H. Liechti-Gallati S, et al. Hum Genet. 1989 Mar;81(4):343-8. doi: 10.1007/BF00283688. Hum Genet. 1989. PMID: 2784778

3

RFLPs for Duchenne muscular dystrophy cDNA clones 9 and 10.

Liechti-Gallati S, Schneider V, Mullis P, Moser H. Liechti-Gallati S, et al. Am J Hum Genet. 1990 Jun;46(6):1090-4. Am J Hum Genet. 1990. PMID: 1971151 Free PMC article.

4

Familial deletion in Becker type muscular dystrophy within the pXJ region.

Liechti-Gallati S, Braga S, Hirsiger H, Moser H. Liechti-Gallati S, et al. Hum Genet. 1987 Nov;77(3):267-8. doi: 10.1007/BF00284483. Hum Genet. 1987. PMID: 2890571

5

[Carrier diagnosis and prenatal prognosis using DNA analysis in X-chromosome-linked Duchenne and Becker muscular dystrophy].

Moser H, Liechti-Gallati S, Braga S, Hirsiger H. Moser H, et al. Schweiz Med Wochenschr. 1987 Dec 19;117(51):2061-73. Schweiz Med Wochenschr. 1987. PMID: 3433090 German.

6

X linked neonatal centronuclear/myotubular myopathy: evidence for linkage to Xq28 DNA marker loci.

Thomas NS, Williams H, Cole G, Roberts K, Clarke A, Liechti-Gallati S, Braga S, Gerber A, Meier C, Moser H, et al. Thomas NS, et al. J Med Genet. 1990 May;27(5):284-7. doi: 10.1136/jmg.27.5.284. J Med Genet. 1990. PMID: 2352256 Free PMC article.

7

Abnormal growth kinetics and 5'-nucleotidase activities in cultured skin fibroblasts from patients with Duchenne muscular dystrophy.

Liechti-Gallati S, Moser H, Siegrist HP, Wiesmann U, Herschkowitz NN. Liechti-Gallati S, et al. Pediatr Res. 1981 Nov;15(11):1411-4. doi: 10.1203/00006450-198111000-00004. Pediatr Res. 1981. PMID: 6272184

8

Distribution of cytoskeletal elements in cultured skin fibroblasts of patients with Duchenne's muscular dystrophy.

Rungger-Brändle E, Liechti-Gallati S, Gabbiani G, Moser H, Herschkowitz N. Rungger-Brändle E, et al. Experientia. 1980 Oct 15;36(10):1204-5. doi: 10.1007/BF01976130. Experientia. 1980. PMID: 6998715

9

Abnormal growth kinetics and 5'-nucleotidase activities in cultured skin fibroblasts from patients with Duchenne muscular dystrophy.

Liechti-Gallati S, Moser H, Siegrist HP, Wiesmann U, Herschkowitz NN. Liechti-Gallati S, et al. Pediatr Res. 1982 Jul;16(7):588. doi: 10.1203/00006450-198207000-00021. Pediatr Res. 1982. PMID: 6287400 No abstract available.

10

The delta F508-deletion in 99 CF patients of Switzerland.

Liechti-Gallati S, Parsai I, Kraemer R, Rudeberg A, Braga S, Moser H. Liechti-Gallati S, et al. Adv Exp Med Biol. 1991;290:367-8. doi: 10.1007/978-1-4684-5934-0_39. Adv Exp Med Biol. 1991. PMID: 1950749 No abstract available.

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