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 F Portnoï

Showing results (11-20 of 14) with videos related to

Pageof 2
Sort By:
You have reached the last page of results.This site can display upto 14 results.
Journal of Medical Genetics|April 16, 1999
Skin pigmentary anomalies and mosaicism for an acentric marker chromosome originating from 3qM F Portnoï, S Boutchneï, F Bouscarat, et al.
Human Reproduction (Oxford, England)|June 6, 2006
Molecular cytogenetic studies of Xq critical regions in premature ovarian failure patientsM F Portnoï, A Aboura, G Tachdjian, et al.
Clinical Genetics|September 27, 2000
Molecular cytogenetic analysis of a duplication Xp in a female with an abnormal phenotype and random X inactivationM F Portnoï, N Bouayed-Abdelmoula, M Mirc, et al.
Prenatal Diagnosis|January 8, 2014
A French collaborative survey of 272 fetuses with 22q11.2 deletion: ultrasound findings, fetal autopsies and pregnancy outcomesJ Besseau-Ayasse, C Violle-Poirsier, A Bazin, et al.
Pageof 2

Showing results (11-20 of 14) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 14 results.
Journal of Medical Genetics|April 16, 1999
Skin pigmentary anomalies and mosaicism for an acentric marker chromosome originating from 3qM F Portnoï, S Boutchneï, F Bouscarat, et al.
Human Reproduction (Oxford, England)|June 6, 2006
Molecular cytogenetic studies of Xq critical regions in premature ovarian failure patientsM F Portnoï, A Aboura, G Tachdjian, et al.
Clinical Genetics|September 27, 2000
Molecular cytogenetic analysis of a duplication Xp in a female with an abnormal phenotype and random X inactivationM F Portnoï, N Bouayed-Abdelmoula, M Mirc, et al.
Prenatal Diagnosis|January 8, 2014
A French collaborative survey of 272 fetuses with 22q11.2 deletion: ultrasound findings, fetal autopsies and pregnancy outcomesJ Besseau-Ayasse, C Violle-Poirsier, A Bazin, et al.
Pageof 2