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

H Tonoki

Showing results (61-70 of 65) with videos related to

Pageof 7
Sort By:
You have reached the last page of results.This site can display upto 65 results.
Human Genetics|October 28, 1997
New p57KIP2 mutations in Beckwith-Wiedemann syndromeI Hatada, A Nabetani, H Morisaki, et al.
Prenatal Diagnosis|January 13, 1999
Prenatal identification of mos 45,X/46,X,+mar in a normal male baby by cytogenetic and molecular analysisN Hoshi, H Tonoki, Y Handa, et al.
American Journal of Medical Genetics|December 26, 2001
No evidence of PEG1/MEST gene mutations in Silver-Russell syndrome patientsS Kobayashi, H Uemura, T Kohda, et al.
Journal of Medical Genetics|July 3, 2008
Lack of C20orf133 and FLRT3 mutations in 43 patients with Kabuki syndrome in JapanH Kuniba, M Tsuda, M Nakashima, et al.
Journal of Medical Genetics|June 26, 2010
Novel and recurrent TRPV4 mutations and their association with distinct phenotypes within the TRPV4 dysplasia familyJ Dai, O-H Kim, T-J Cho, et al.
Pageof 7

Showing results (61-70 of 65) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 65 results.
Human Genetics|October 28, 1997
New p57KIP2 mutations in Beckwith-Wiedemann syndromeI Hatada, A Nabetani, H Morisaki, et al.
Prenatal Diagnosis|January 13, 1999
Prenatal identification of mos 45,X/46,X,+mar in a normal male baby by cytogenetic and molecular analysisN Hoshi, H Tonoki, Y Handa, et al.
American Journal of Medical Genetics|December 26, 2001
No evidence of PEG1/MEST gene mutations in Silver-Russell syndrome patientsS Kobayashi, H Uemura, T Kohda, et al.
Journal of Medical Genetics|July 3, 2008
Lack of C20orf133 and FLRT3 mutations in 43 patients with Kabuki syndrome in JapanH Kuniba, M Tsuda, M Nakashima, et al.
Journal of Medical Genetics|June 26, 2010
Novel and recurrent TRPV4 mutations and their association with distinct phenotypes within the TRPV4 dysplasia familyJ Dai, O-H Kim, T-J Cho, et al.
Pageof 7