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

G Pierquin

Showing results (11-20 of 17) with videos related to

Pageof 2
Sort By:
You have reached the last page of results.This site can display upto 17 results.
Genetic Counseling (Geneva, Switzerland)|April 30, 2009
Deletion of Xpter encompassing the SHOX gene and PAR1 region in familial patients with Leri-Weill Dyschondrosteosis syndromeL Mutesa, J F Vanbellinghen, A C Hellin, et al.
Genetic Counseling (Geneva, Switzerland)|September 17, 2013
Clinical, cytogenetic and molecular characterization of two cases of mosaic ring chromosome 13A Uwineza, G Pierquin, S Gaillez, et al.
American Journal of Medical Genetics|April 10, 1995
Severe Smith-Lemli-Opitz syndrome with prolonged survival and lipid abnormalitiesG Pierquin, P Peeters, F Roels, et al.
Human Genetics|September 1, 1991
Two unrelated children with partial trisomy 1q and monosomy 6p, presenting with the phenotype of the Larsen syndromeG Pierquin, N Van Regemorter, Hayez-Delatte, et al.
Clinical Genetics|November 19, 2016
Autosomal recessive variations of TBX6, from congenital scoliosis to spondylocostal dysostosisM Lefebvre, Y Duffourd, T Jouan, et al.
Human Mutation|March 17, 2010
FOXL2 copy number changes in the molecular pathogenesis of BPES: unique cohort of 17 deletionsB D'haene, J Nevado, M Pugeat, et al.
Molecular Syndromology|November 4, 2010
IRF6 Screening of Syndromic and a priori Non-Syndromic Cleft Lip and Palate Patients: Identification of a New Type of Minor VWS SignL Desmyter, M Ghassibe, N Revencu, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Genetic Counseling (Geneva, Switzerland)|April 30, 2009
Deletion of Xpter encompassing the SHOX gene and PAR1 region in familial patients with Leri-Weill Dyschondrosteosis syndromeL Mutesa, J F Vanbellinghen, A C Hellin, et al.
Genetic Counseling (Geneva, Switzerland)|September 17, 2013
Clinical, cytogenetic and molecular characterization of two cases of mosaic ring chromosome 13A Uwineza, G Pierquin, S Gaillez, et al.
American Journal of Medical Genetics|April 10, 1995
Severe Smith-Lemli-Opitz syndrome with prolonged survival and lipid abnormalitiesG Pierquin, P Peeters, F Roels, et al.
Human Genetics|September 1, 1991
Two unrelated children with partial trisomy 1q and monosomy 6p, presenting with the phenotype of the Larsen syndromeG Pierquin, N Van Regemorter, Hayez-Delatte, et al.
Clinical Genetics|November 19, 2016
Autosomal recessive variations of TBX6, from congenital scoliosis to spondylocostal dysostosisM Lefebvre, Y Duffourd, T Jouan, et al.
Human Mutation|March 17, 2010
FOXL2 copy number changes in the molecular pathogenesis of BPES: unique cohort of 17 deletionsB D'haene, J Nevado, M Pugeat, et al.
Molecular Syndromology|November 4, 2010
IRF6 Screening of Syndromic and a priori Non-Syndromic Cleft Lip and Palate Patients: Identification of a New Type of Minor VWS SignL Desmyter, M Ghassibe, N Revencu, et al.
Pageof 2