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

Ewa Zietkiewicz

Showing results (11-20 of 18) with videos related to

Pageof 2
Sort By:
You have reached the last page of results.This site can display upto 18 results.
European Journal of Human Genetics : EJHG|February 14, 2008
Sequence analysis of 21 genes located in the Kartagener syndrome linkage region on chromosome 15qMaciej Geremek, Frederieke Schoenmaker, Ewa Zietkiewicz, et al.
Journal of Applied Genetics|December 19, 2023
The effect of library preparation protocol on the efficiency of heteroplasmy detection in mitochondrial DNA using two massively parallel sequencing Illumina systemsPatrycja Daca-Roszak, Joanna Fiedorowicz, Maciej Jankowski, et al.
Journal of Medical Genetics|August 2, 2019
Truncating mutations in exons 20 and 21 of <i>OFD1</i> can cause primary ciliary dyskinesia without associated syndromic symptomsZuzanna Bukowy-Bieryllo, Alicja Rabiasz, Maciej Dabrowski, et al.
American Journal of Respiratory Cell and Molecular Biology|March 28, 2019
<i>CFAP300</i>: Mutations in Slavic Patients with Primary Ciliary Dyskinesia and a Role in Ciliary Dynein Arms TraffickingEwa Zietkiewicz, Zuzanna Bukowy-Bieryllo, Alicja Rabiasz, et al.
European Journal of Human Genetics : EJHG|October 16, 2003
Human X-chromosomal lineages in Europe reveal Middle Eastern and Asiatic contactsFeng-Xia Xiao, Vania Yotova, Ewa Zietkiewicz, et al.
American Journal of Human Genetics|September 27, 2003
Haplotypes in the dystrophin DNA segment point to a mosaic origin of modern human diversityEwa Zietkiewicz, Vania Yotova, Dominik Gehl, et al.
Human Genetics|May 11, 2005
Anatomy of a founder effect: myotonic dystrophy in Northeastern QuebecVania Yotova, Damian Labuda, Ewa Zietkiewicz, et al.
American Journal of Human Genetics|October 28, 2008
DNAI2 mutations cause primary ciliary dyskinesia with defects in the outer dynein armNiki Tomas Loges, Heike Olbrich, Lale Fenske, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
European Journal of Human Genetics : EJHG|February 14, 2008
Sequence analysis of 21 genes located in the Kartagener syndrome linkage region on chromosome 15qMaciej Geremek, Frederieke Schoenmaker, Ewa Zietkiewicz, et al.
Journal of Applied Genetics|December 19, 2023
The effect of library preparation protocol on the efficiency of heteroplasmy detection in mitochondrial DNA using two massively parallel sequencing Illumina systemsPatrycja Daca-Roszak, Joanna Fiedorowicz, Maciej Jankowski, et al.
Journal of Medical Genetics|August 2, 2019
Truncating mutations in exons 20 and 21 of <i>OFD1</i> can cause primary ciliary dyskinesia without associated syndromic symptomsZuzanna Bukowy-Bieryllo, Alicja Rabiasz, Maciej Dabrowski, et al.
American Journal of Respiratory Cell and Molecular Biology|March 28, 2019
<i>CFAP300</i>: Mutations in Slavic Patients with Primary Ciliary Dyskinesia and a Role in Ciliary Dynein Arms TraffickingEwa Zietkiewicz, Zuzanna Bukowy-Bieryllo, Alicja Rabiasz, et al.
European Journal of Human Genetics : EJHG|October 16, 2003
Human X-chromosomal lineages in Europe reveal Middle Eastern and Asiatic contactsFeng-Xia Xiao, Vania Yotova, Ewa Zietkiewicz, et al.
American Journal of Human Genetics|September 27, 2003
Haplotypes in the dystrophin DNA segment point to a mosaic origin of modern human diversityEwa Zietkiewicz, Vania Yotova, Dominik Gehl, et al.
Human Genetics|May 11, 2005
Anatomy of a founder effect: myotonic dystrophy in Northeastern QuebecVania Yotova, Damian Labuda, Ewa Zietkiewicz, et al.
American Journal of Human Genetics|October 28, 2008
DNAI2 mutations cause primary ciliary dyskinesia with defects in the outer dynein armNiki Tomas Loges, Heike Olbrich, Lale Fenske, et al.
Pageof 2