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B Dworniczak

Showing results (41-50 of 48) with videos related to

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Human Genetics|June 1, 1995
Genetic heterogeneity of polycystic kidney disease in BulgariaN Bogdanova, B Dworniczak, D Dragova, et al.
Journal of Medical Genetics|October 1, 1991
Silent mutations in the phenylalanine hydroxylase gene as an aid to the diagnosis of phenylketonuriaL Kalaydjieva, B Dworniczak, C Aulehla-Scholz, et al.
American Journal of Medical Genetics|May 22, 1995
Parental origin of the extra haploid chromosome set in triploidies diagnosed prenatallyP Miny, B Koppers, B Dworniczak, et al.
Human Mutation|August 3, 2000
Screening the 3' region of the polycystic kidney disease 1 (PKD1) gene in 41 Bulgarian and Australian kindreds reveals a prevalence of protein truncating mutationsN Bogdanova, M McCluskey, K Sikmann, et al.
Fertility and Sterility|March 1, 1997
Screening for deletions of the Y chromosome involving the DAZ (Deleted in AZoospermia) gene in azoospermia and severe oligozoospermiaM Simoni, J Gromoll, B Dworniczak, et al.
American Journal of Human Genetics|December 1, 1999
A 28-kb deletion spanning D15S63 (PW71) in five families: a rare neutral variant?K Buiting, B Dittrich, B Dworniczak, et al.
Human Genetics|September 1, 1997
Distinct spectrum of CFTR gene mutations in congenital absence of vas deferensT Dörk, B Dworniczak, C Aulehla-Scholz, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|December 26, 2001
Angiotensin-converting enzyme activity and the ACE Alu polymorphism in autosomal dominant polycystic kidney diseaseT Schiavello, V Burke, N Bogdanova, et al.
Pageof 5

Showing results (41-50 of 48) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 48 results.
Human Genetics|June 1, 1995
Genetic heterogeneity of polycystic kidney disease in BulgariaN Bogdanova, B Dworniczak, D Dragova, et al.
Journal of Medical Genetics|October 1, 1991
Silent mutations in the phenylalanine hydroxylase gene as an aid to the diagnosis of phenylketonuriaL Kalaydjieva, B Dworniczak, C Aulehla-Scholz, et al.
American Journal of Medical Genetics|May 22, 1995
Parental origin of the extra haploid chromosome set in triploidies diagnosed prenatallyP Miny, B Koppers, B Dworniczak, et al.
Human Mutation|August 3, 2000
Screening the 3' region of the polycystic kidney disease 1 (PKD1) gene in 41 Bulgarian and Australian kindreds reveals a prevalence of protein truncating mutationsN Bogdanova, M McCluskey, K Sikmann, et al.
Fertility and Sterility|March 1, 1997
Screening for deletions of the Y chromosome involving the DAZ (Deleted in AZoospermia) gene in azoospermia and severe oligozoospermiaM Simoni, J Gromoll, B Dworniczak, et al.
American Journal of Human Genetics|December 1, 1999
A 28-kb deletion spanning D15S63 (PW71) in five families: a rare neutral variant?K Buiting, B Dittrich, B Dworniczak, et al.
Human Genetics|September 1, 1997
Distinct spectrum of CFTR gene mutations in congenital absence of vas deferensT Dörk, B Dworniczak, C Aulehla-Scholz, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|December 26, 2001
Angiotensin-converting enzyme activity and the ACE Alu polymorphism in autosomal dominant polycystic kidney diseaseT Schiavello, V Burke, N Bogdanova, et al.
Pageof 5