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B Dworniczak

Showing results (31-40 of 48) with videos related to

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Lancet (London, England)|February 11, 1989
Direct sequencing of amplified DNA in prenatal diagnosis of beta-thalassaemiaC Aulehla-Scholz, R Spiegelberg, P Miny, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Comparison of conformation-sensitive gel electrophoresis and single-strand conformation polymorphism analysis for detection of mutations in the BRCA1 gene using optimized conformation analysis protocolsA Markoff, H Sormbroen, N Bogdanova, et al.
American Journal of Human Genetics|November 5, 1997
CFTR gene mutations in men with bilateral ejaculatory-duct obstruction and anomalies of the seminal vesiclesD Meschede, B Dworniczak, H M Behre, et al.
Lancet (London, England)|April 6, 1991
Phenylketonuria mutation in southern EuropeansL Kalaydjieva, B Dworniczak, C Aulehla-Scholz, et al.
Human Genetics|October 1, 1991
Recurrent nonsense mutation in exon 7 of the phenylalanine hydroxylase geneB Dworniczak, L Kalaydjieva, C Aulehla-Scholz, et al.
Gut|July 1, 2005
Complete cystic fibrosis transmembrane conductance regulator gene sequencing in patients with idiopathic chronic pancreatitis and controlsF U Weiss, P Simon, N Bogdanova, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|June 10, 2011
Bcar3 is expressed in sertoli cells and germ cells of the developing testis in miceP Pennekamp, S Feldner, F J Seesing, et al.
Human Genetics|September 1, 1990
The frequency of the CF delta F508 deletion in CF chromosomes of different ethnic originC Aulehla-Scholz, R Kaiser, J Weber, et al.
Clinical Genetics|March 1, 1992
Heterogeneity of mutations in Bulgarian phenylketonuria haplotype 1 and 4 allelesL Kalaydjieva, B Dworniczak, I Kremensky, et al.
Human Mutation|January 1, 1992
Two missense mutations causing mild hyperphenylalaninemia associated with DNA haplotype 12E Svensson, R C Eisensmith, B Dworniczak, et al.
Pageof 5

Showing results (31-40 of 48) with videos related to

Sort By:
Pageof 5
Lancet (London, England)|February 11, 1989
Direct sequencing of amplified DNA in prenatal diagnosis of beta-thalassaemiaC Aulehla-Scholz, R Spiegelberg, P Miny, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Comparison of conformation-sensitive gel electrophoresis and single-strand conformation polymorphism analysis for detection of mutations in the BRCA1 gene using optimized conformation analysis protocolsA Markoff, H Sormbroen, N Bogdanova, et al.
American Journal of Human Genetics|November 5, 1997
CFTR gene mutations in men with bilateral ejaculatory-duct obstruction and anomalies of the seminal vesiclesD Meschede, B Dworniczak, H M Behre, et al.
Lancet (London, England)|April 6, 1991
Phenylketonuria mutation in southern EuropeansL Kalaydjieva, B Dworniczak, C Aulehla-Scholz, et al.
Human Genetics|October 1, 1991
Recurrent nonsense mutation in exon 7 of the phenylalanine hydroxylase geneB Dworniczak, L Kalaydjieva, C Aulehla-Scholz, et al.
Gut|July 1, 2005
Complete cystic fibrosis transmembrane conductance regulator gene sequencing in patients with idiopathic chronic pancreatitis and controlsF U Weiss, P Simon, N Bogdanova, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|June 10, 2011
Bcar3 is expressed in sertoli cells and germ cells of the developing testis in miceP Pennekamp, S Feldner, F J Seesing, et al.
Human Genetics|September 1, 1990
The frequency of the CF delta F508 deletion in CF chromosomes of different ethnic originC Aulehla-Scholz, R Kaiser, J Weber, et al.
Clinical Genetics|March 1, 1992
Heterogeneity of mutations in Bulgarian phenylketonuria haplotype 1 and 4 allelesL Kalaydjieva, B Dworniczak, I Kremensky, et al.
Human Mutation|January 1, 1992
Two missense mutations causing mild hyperphenylalaninemia associated with DNA haplotype 12E Svensson, R C Eisensmith, B Dworniczak, et al.
Pageof 5