Moser H - 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. Among authors: moser h. Hum Genet. 1989 Mar;81(4):343-8. doi: 10.1007/BF00283688. Hum Genet. 1989. PMID: 2784778

2

RFLPs for Duchenne muscular dystrophy cDNA clones 9 and 10.

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

3

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. Among authors: moser h. Clin Genet. 1990 Jun;37(6):442-9. doi: 10.1111/j.1399-0004.1990.tb03528.x. Clin Genet. 1990. PMID: 1974485

4

The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion.

Koenig M, Beggs AH, Moyer M, Scherpf S, Heindrich K, Bettecken T, Meng G, Müller CR, Lindlöf M, Kaariainen H, de la Chapellet A, Kiuru A, Savontaus ML, Gilgenkrantz H, Récan D, Chelly J, Kaplan JC, Covone AE, Archidiacono N, Romeo G, Liechti-Gailati S, Schneider V, Braga S, Moser H, Darras BT, Murphy P, Francke U, Chen JD, Morgan G, Denton M, Greenberg CR, Wrogemann K, Blonden LA, van Paassen MB, van Ommen GJ, Kunkel LM. Koenig M, et al. Among authors: moser h. Am J Hum Genet. 1989 Oct;45(4):498-506. Am J Hum Genet. 1989. PMID: 2491009 Free PMC article.

5

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. Among authors: moser h. Hum Genet. 1987 Nov;77(3):267-8. doi: 10.1007/BF00284483. Hum Genet. 1987. PMID: 2890571

6

[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.

7

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. Among authors: moser h. Neuromuscul Disord. 1991;1(4):239-45. doi: 10.1016/0960-8966(91)90096-b. Neuromuscul Disord. 1991. PMID: 1822801

8

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. Among authors: moser h. 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.

9

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. Among authors: moser h. Genomics. 1988 Jan;2(1):90-5. doi: 10.1016/0888-7543(88)90113-9. Genomics. 1988. PMID: 3384440

10

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. Among authors: moser h. Hum Genet. 1993 Mar;91(1):55-62. doi: 10.1007/BF00230223. Hum Genet. 1993. PMID: 8454288

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