Dworniczak B - Search Results

1

Complete cystic fibrosis transmembrane conductance regulator gene sequencing in patients with idiopathic chronic pancreatitis and controls.

Weiss FU, Simon P, Bogdanova N, Mayerle J, Dworniczak B, Horst J, Lerch MM. Weiss FU, et al. Among authors: dworniczak b. Gut. 2005 Oct;54(10):1456-60. doi: 10.1136/gut.2005.064808. Epub 2005 Jun 29. Gut. 2005. PMID: 15987793 Free PMC article.

2

Genetic diseases of the seminal ducts.

Meschede D, Dworniczak B, Nieschlag E, Horst J. Meschede D, et al. Among authors: dworniczak b. Biomed Pharmacother. 1998;52(5):197-203. doi: 10.1016/S0753-3322(98)80016-4. Biomed Pharmacother. 1998. PMID: 9755815 Review.

3

Prevalence of small rearrangements in the factor VIII gene F8C among patients with severe hemophilia A.

Bogdanova N, Markoff A, Pollmann H, Nowak-Göttl U, Eisert R, Dworniczak B, Eigel A, Horst J. Bogdanova N, et al. Among authors: dworniczak b. Hum Mutat. 2002 Sep;20(3):236-7. doi: 10.1002/humu.9062. Hum Mutat. 2002. PMID: 12204009

4

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. Among authors: dworniczak b. Hum Genet. 1991 Oct;87(6):739-41. doi: 10.1007/BF00201738. Hum Genet. 1991. PMID: 1682235

5

Phenylalanine hydroxylase gene: silent mutation uncovers evolutionary origin of different alleles.

Dworniczak B, Aulehla-Scholz C, Horst J. Dworniczak B, et al. Clin Genet. 1990 Oct;38(4):270-3. doi: 10.1111/j.1399-0004.1990.tb03580.x. Clin Genet. 1990. PMID: 2268974

6

Phenylketonuria: detection of a frequent haplotype 4 allele mutation.

Dworniczak B, Aulehla-Scholz C, Horst J. Dworniczak B, et al. Hum Genet. 1989 Dec;84(1):95-6. doi: 10.1007/BF00210683. Hum Genet. 1989. PMID: 2606484

7

Distinct spectrum of CFTR gene mutations in congenital absence of vas deferens.

Dörk T, Dworniczak B, Aulehla-Scholz C, Wieczorek D, Böhm I, Mayerova A, Seydewitz HH, Nieschlag E, Meschede D, Horst J, Pander HJ, Sperling H, Ratjen F, Passarge E, Schmidtke J, Stuhrmann M. Dörk T, et al. Among authors: dworniczak b. Hum Genet. 1997 Sep;100(3-4):365-77. doi: 10.1007/s004390050518. Hum Genet. 1997. PMID: 9272157

8

Comparison of conformation-sensitive gel electrophoresis and single-strand conformation polymorphism analysis for detection of mutations in the BRCA1 gene using optimized conformation analysis protocols.

Markoff A, Sormbroen H, Bogdanova N, Preisler-Adams S, Ganev V, Dworniczak B, Horst J. Markoff A, et al. Among authors: dworniczak b. Eur J Hum Genet. 1998 Mar-Apr;6(2):145-50. doi: 10.1038/sj.ejhg.5200171. Eur J Hum Genet. 1998. PMID: 9781059

9

Seven novel and four recurrent point mutations in the factor VIII (F8C) gene.

Bogdanova N, Lemcke B, Markoff A, Pollmann H, Dworniczak B, Eigel A, Horst J. Bogdanova N, et al. Among authors: dworniczak b. Hum Mutat. 2001 Dec;18(6):546. doi: 10.1002/humu.1234. Hum Mutat. 2001. PMID: 11748850

10

Seven novel and four recurrent point mutations in the factor VIII (F8C) gene.

Bogdanova N, Lemcke B, Markoff A, Pollmann H, Dworniczak B, Eigel A, Horst J. Bogdanova N, et al. Among authors: dworniczak b. Hum Mutat. 2002 Jan;19(1):84. doi: 10.1002/humu.9007. Hum Mutat. 2002. PMID: 11754115

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

99 results

Search Page

Filters