Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

M Zygulska

Showing results (1-10 of 9) with videos related to

Pageof 1
Sort By:
Human Genetics|May 1, 1993
FFU complex: an analysis of 491 casesW Lenz, M Zygulska, J Horst
Human Mutation|January 1, 1994
Phenylketonuria in southern Poland: a new splice mutation in intron 9 at the PAH locusM Zygulska, A Eigel, J J Pietrzyk, et al.
Human Mutation|January 1, 1993
Phenylalanine hydroxylase gene: a novel splice mutation in intron 2 in two German and Polish families with severe phenylketonuriaM Zygulska, A Eigel, J J Pietrzyk, et al.
Human Mutation|January 1, 1993
A novel mutation in exon 8 of the phenylalanine hydroxylase gene in the Polish populationM Zygulska, A Eigel, J J Pietrzyk, et al.
Pediatria Polska|March 1, 1987
[Clefts of the primary palate and secondary palate. I. Empirical and relative risks of the development of the defects]J J Pietrzyk, B S Rózański, E Swisterska, et al.
Pediatria Polska|March 1, 1987
[Clefts of the primary palate and secondary palate. II. Evaluation of the mode of inheritance]J J Pietrzyk, B S Rózański, E Swisterska, et al.
Human Genetics|January 1, 1991
Molecular analysis of PKU haplotypes in the population of southern PolandM Zygulska, A Eigel, C Aulehla-Scholz, 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.
Acta Biochimica Polonica|January 1, 1996
Analysis of unstable DNA sequence in FMR1 gene in Polish families with fragile X syndromeM Milewski, M Zygulska, J Bal, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Human Genetics|May 1, 1993
FFU complex: an analysis of 491 casesW Lenz, M Zygulska, J Horst
Human Mutation|January 1, 1994
Phenylketonuria in southern Poland: a new splice mutation in intron 9 at the PAH locusM Zygulska, A Eigel, J J Pietrzyk, et al.
Human Mutation|January 1, 1993
Phenylalanine hydroxylase gene: a novel splice mutation in intron 2 in two German and Polish families with severe phenylketonuriaM Zygulska, A Eigel, J J Pietrzyk, et al.
Human Mutation|January 1, 1993
A novel mutation in exon 8 of the phenylalanine hydroxylase gene in the Polish populationM Zygulska, A Eigel, J J Pietrzyk, et al.
Pediatria Polska|March 1, 1987
[Clefts of the primary palate and secondary palate. I. Empirical and relative risks of the development of the defects]J J Pietrzyk, B S Rózański, E Swisterska, et al.
Pediatria Polska|March 1, 1987
[Clefts of the primary palate and secondary palate. II. Evaluation of the mode of inheritance]J J Pietrzyk, B S Rózański, E Swisterska, et al.
Human Genetics|January 1, 1991
Molecular analysis of PKU haplotypes in the population of southern PolandM Zygulska, A Eigel, C Aulehla-Scholz, 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.
Acta Biochimica Polonica|January 1, 1996
Analysis of unstable DNA sequence in FMR1 gene in Polish families with fragile X syndromeM Milewski, M Zygulska, J Bal, et al.
Pageof 1