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B Dworniczak

Showing results (21-30 of 48) with videos related to

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Genomics|June 21, 2001
Homologues to the first gene for autosomal dominant polycystic kidney disease are pseudogenesN Bogdanova, A Markoff, V Gerke, et al.
Human Genetics|February 1, 1991
Geographical distribution gradients of the major PKU mutations and the linked haplotypesL Kalaydjieva, B Dworniczak, V Kucinskas, et al.
Genomics|October 1, 1991
Aberrant splicing of phenylalanine hydroxylase mRNA: the major cause for phenylketonuria in parts of southern EuropeB Dworniczak, C Aulehla-Scholz, L Kalaydjieva, et al.
Human Mutation|January 1, 1992
Analysis of exon 7 of the human phenylalanine hydroxylase gene: a mutation hot spot?B Dworniczak, L Kalaydjieva, S Pankoke, et al.
Genomics|January 1, 1991
Phenylalanine hydroxylase gene: novel missense mutation in exon 7 causing severe phenylketonuriaB Dworniczak, K Grudda, J Stümper, et al.
Human Genetics|November 1, 1991
Phenylketonuria in Poland: 66% of PKU alleles are caused by three mutationsM Zygulska, A Eigel, B Dworniczak, et al.
Nucleic Acids Research|May 11, 1991
Non-isotopic detection of single strand conformation polymorphism (PCR-SSCP): a rapid and sensitive technique in diagnosis of phenylketonuriaB Dockhorn-Dworniczak, B Dworniczak, L Brömmelkamp, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|August 26, 1998
Characterization of the murine polycystic kidney disease (Pkd2) geneP Pennekamp, N Bogdanova, M Wilda, et al.
Human Mutation|December 19, 2001
Seven novel and four recurrent point mutations in the factor VIII (F8C) geneN Bogdanova, B Lemcke, A Markoff, et al.
Journal of Medical Genetics|December 1, 1990
Classical phenylketonuria in Bulgaria: RFLP haplotypes and frequency of the major mutationsL Kalaydjieva, B Dworniczak, C Aulehla-Scholz, et al.
Pageof 5

Showing results (21-30 of 48) with videos related to

Sort By:
Pageof 5
Genomics|June 21, 2001
Homologues to the first gene for autosomal dominant polycystic kidney disease are pseudogenesN Bogdanova, A Markoff, V Gerke, et al.
Human Genetics|February 1, 1991
Geographical distribution gradients of the major PKU mutations and the linked haplotypesL Kalaydjieva, B Dworniczak, V Kucinskas, et al.
Genomics|October 1, 1991
Aberrant splicing of phenylalanine hydroxylase mRNA: the major cause for phenylketonuria in parts of southern EuropeB Dworniczak, C Aulehla-Scholz, L Kalaydjieva, et al.
Human Mutation|January 1, 1992
Analysis of exon 7 of the human phenylalanine hydroxylase gene: a mutation hot spot?B Dworniczak, L Kalaydjieva, S Pankoke, et al.
Genomics|January 1, 1991
Phenylalanine hydroxylase gene: novel missense mutation in exon 7 causing severe phenylketonuriaB Dworniczak, K Grudda, J Stümper, et al.
Human Genetics|November 1, 1991
Phenylketonuria in Poland: 66% of PKU alleles are caused by three mutationsM Zygulska, A Eigel, B Dworniczak, et al.
Nucleic Acids Research|May 11, 1991
Non-isotopic detection of single strand conformation polymorphism (PCR-SSCP): a rapid and sensitive technique in diagnosis of phenylketonuriaB Dockhorn-Dworniczak, B Dworniczak, L Brömmelkamp, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|August 26, 1998
Characterization of the murine polycystic kidney disease (Pkd2) geneP Pennekamp, N Bogdanova, M Wilda, et al.
Human Mutation|December 19, 2001
Seven novel and four recurrent point mutations in the factor VIII (F8C) geneN Bogdanova, B Lemcke, A Markoff, et al.
Journal of Medical Genetics|December 1, 1990
Classical phenylketonuria in Bulgaria: RFLP haplotypes and frequency of the major mutationsL Kalaydjieva, B Dworniczak, C Aulehla-Scholz, et al.
Pageof 5