Eigel A - Search Results

1

The frequency of the CF delta F508 deletion in CF chromosomes of different ethnic origin.

Aulehla-Scholz C, Kaiser R, Weber J, Pivetta O, Eigel A, Dworniczak B, Olek K, Horst J. Aulehla-Scholz C, et al. Among authors: eigel a. Hum Genet. 1990 Sep;85(4):392-3. doi: 10.1007/BF02428269. Hum Genet. 1990. PMID: 2210740 No abstract available.

2

A frameshift mutation in exon 2 of the phenylalanine hydroxylase gene linked to RFLP haplotype 1.

Eigel A, Dworniczak B, Kalaydjieva L, Horst J. Eigel A, et al. Hum Genet. 1991 Oct;87(6):739-41. doi: 10.1007/BF00201738. Hum Genet. 1991. PMID: 1682235

3

Hb D Los Angeles (D-Punjab) and Hb Presbyterian: analysis of the defect at the DNA level.

Schnee J, Aulehla-Scholz C, Eigel A, Horst J. Schnee J, et al. Among authors: eigel a. Hum Genet. 1990 Mar;84(4):365-7. doi: 10.1007/BF00196236. Hum Genet. 1990. PMID: 2307460

4

Mutation analysis of beta-thalassemia genes in a German family reveals a rare transversion in the first intron.

Eigel A, Schnee J, Oehme R, Horst J. Eigel A, et al. Hum Genet. 1989 Mar;81(4):371-2. doi: 10.1007/BF00283694. Hum Genet. 1989. PMID: 2703241

5

Identification of a single nucleotide C-to-T transition and five different deletions in patients with severe hemophilia B.

Ludwig M, Schwaab R, Eigel A, Horst J, Egli H, Brackmann HH, Olek K. Ludwig M, et al. Among authors: eigel a. Am J Hum Genet. 1989 Jul;45(1):115-22. Am J Hum Genet. 1989. PMID: 2741941 Free PMC article.

6

Cystic fibrosis: typing 89 German families with linked DNA probes.

Weber J, Aulehla-Scholz C, Kaiser R, Eigel A, Neugebauer M, Horst J, Olek K. Weber J, et al. Among authors: eigel a. Hum Genet. 1988 Dec;81(1):54-6. doi: 10.1007/BF00283729. Hum Genet. 1988. PMID: 2904405

7

Nonisotopic detection of mutations using a modified single-strand conformation polymorphism analysis.

Weidner J, Eigel A, Horst J, Köhnlein W. Weidner J, et al. Among authors: eigel a. Hum Mutat. 1994;4(1):55-6. doi: 10.1002/humu.1380040108. Hum Mutat. 1994. PMID: 7524914

8

Compound heterozygosity for the delta F508 and F508C cystic fibrosis transmembrane conductance regulator (CFTR) mutations in a patient with congenital bilateral aplasia of the vas deferens.

Meschede D, Eigel A, Horst J, Nieschlag E. Meschede D, et al. Among authors: eigel a. Am J Hum Genet. 1993 Jul;53(1):292-3. Am J Hum Genet. 1993. PMID: 7686336 Free PMC article. No abstract available.

9

Geographic distribution and origin of CFTR mutations in Germany.

Tümmler B, Storrs T, Dziadek V, Dörk T, Meitinger T, Golla A, Bertele-Harms RM, Harms HK, Schröder E, Claass A, Rutjes J, Schneppenheim R, Bauer I, Breuel K, Stuhrmann M, Schmidtke J, Lindner M, Eigel A, Horst J, Kaiser R, Lentze MJ, Schmidt K, von der Hardt H, Estivill X. Tümmler B, et al. Among authors: eigel a. Hum Genet. 1996 Jun;97(6):727-31. doi: 10.1007/BF02346181. Hum Genet. 1996. PMID: 8641688

10

Prevalence of alpha-thalassemias in northern Thailand.

Lemmens-Zygulska M, Eigel A, Helbig B, Sanguansermsri T, Horst J, Flatz G. Lemmens-Zygulska M, et al. Among authors: eigel a. Hum Genet. 1996 Sep;98(3):345-7. doi: 10.1007/s004390050220. Hum Genet. 1996. PMID: 8707307

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