Liechti-Gallati S - Search Results

1

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

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

Association between haplotypes and specific mutations in Swiss cystic fibrosis families.

Liechti-Gallati S, Malik N, Alkan M, Maechler M, Morris M, Thonney F, Sennhauser F, Moser H. Liechti-Gallati S, et al. Pediatr Res. 1991 Oct;30(4):304-8. doi: 10.1203/00006450-199110000-00003. Pediatr Res. 1991. PMID: 1683481

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

Screening for carriers of cystic fibrosis among partners of people heterozygous for the disease.

Sennhauser FH, Liechti-Gallati S, Moser H. Sennhauser FH, et al. BMJ. 1990 Nov 10;301(6760):1081. doi: 10.1136/bmj.301.6760.1081. BMJ. 1990. PMID: 2103736 Free PMC article. No abstract available.

6

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

7

Prenatal diagnosis of X-linked centronuclear myopathy by linkage analysis.

Liechti-Gallati S, Wolff G, Ketelsen UP, Braga S. Liechti-Gallati S, et al. Pediatr Res. 1993 Feb;33(2):201-4. doi: 10.1203/00006450-199302000-00022. Pediatr Res. 1993. PMID: 8433896

8

A new mutation, 3905insT, accounts for 4.8% of 1173 CF chromosomes in Switzerland and causes a severe phenotype.

Hergersberg M, Balakrishnan J, Bettecken T, Chevalier-Porst F, Brägger C, Burger R, Einschenk I, Liechti-Gallati S, Morris M, Schorderet D, Thonney F, Moser H, Malik N. Hergersberg M, et al. Hum Genet. 1997 Aug;100(2):220-3. doi: 10.1007/s004390050494. Hum Genet. 1997. PMID: 9254853

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

An EcoRI polymorphism for the glutaminyl-tRNA synthetase (QARS) gene on chromosome 1q.

Sander AK, Liechti-Gallati S, Kunze N, Moser H, Zingg M, Raveh J. Sander AK, et al. Hum Mol Genet. 1992 Jul;1(4):288. doi: 10.1093/hmg/1.4.288. Hum Mol Genet. 1992. PMID: 1363872 No abstract available.

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