Liechti-Gallati S - Search Results

1

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

2

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

3

[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.

4

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.

5

Haplotype analysis for CF-linked DNA polymorphisms in Switzerland.

Liechti-Gallati S, Niederer BU, Schneider V, Mächler M, Alkan M, Malik N, Braga S, Moser H. Liechti-Gallati S, et al. Clin Genet. 1990 Jun;37(6):442-9. doi: 10.1111/j.1399-0004.1990.tb03528.x. Clin Genet. 1990. PMID: 1974485

6

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

7

Linkage of Van der Woude syndrome (VWS) to REN and exclusion of the candidate gene TGFB2 from the disease locus in a large pedigree.

Sander A, Moser H, Liechti-Gallati S, Grimm T, Zingg M, Raveh J. Sander A, et al. Hum Genet. 1993 Mar;91(1):55-62. doi: 10.1007/BF00230223. Hum Genet. 1993. PMID: 8454288

8

Detection and characterization of mitochondrial DNA rearrangements in Pearson and Kearns-Sayre syndromes by long PCR.

Kleinle S, Wiesmann U, Superti-Furga A, Krähenbühl S, Boltshauser E, Reichen J, Liechti-Gallati S. Kleinle S, et al. Hum Genet. 1997 Oct;100(5-6):643-50. doi: 10.1007/s004390050567. Hum Genet. 1997. PMID: 9341886

9

Two buffer PAGE system-based SSCP/HD analysis: a general protocol for rapid and sensitive mutation screening in cystic fibrosis and any other human genetic disease.

Liechti-Gallati S, Schneider V, Neeser D, Kraemer R. Liechti-Gallati S, et al. Eur J Hum Genet. 1999 Jul;7(5):590-8. doi: 10.1038/sj.ejhg.5200338. Eur J Hum Genet. 1999. PMID: 10439967

10

X-linked centronuclear myopathy: mapping the gene to Xq28.

Liechti-Gallati S, Müller B, Grimm T, Kress W, Müller C, Boltshauser E, Moser H, Braga S. Liechti-Gallati S, et al. Neuromuscul Disord. 1991;1(4):239-45. doi: 10.1016/0960-8966(91)90096-b. Neuromuscul Disord. 1991. PMID: 1822801

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