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 Vekemans

Showing results (251-260 of 289) with videos related to

Pageof 29
Sort By:
The Journal of Pediatrics|July 11, 2001
Inversion of the circadian rhythm of melatonin in the Smith-Magenis syndromeH De Leersnyder, M C De Blois, B Claustrat, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|September 28, 2011
[Preimplantation diagnosis with HLA typing: birth of the first double hope child in France]F Lamazou, J Steffann, N Frydman, et al.
Clinical Genetics|October 12, 2001
Comparative genomic hybridisation in mentally retarded patients with dysmorphic features and a normal karyotypeG Joly, J M Lapierre, C Ozilou, et al.
Clinical Genetics|October 16, 2012
Monozygotic twins discordant for submicroscopic chromosomal anomalies in 2p25.3 region detected by array CGHM Rio, G Royer, S Gobin, et al.
Journal of the American Society for Mass Spectrometry|November 14, 2013
False results caused by solvent impurity in tetrahydrofuran for MALDI TOF MS analysis of aminesXianwen Lou, Christianus M A Leenders, Arthur H A M van Onzen, et al.
Clinical Genetics|April 10, 2002
A CGH study of 27 patients with CHARGE associationD Sanlaville, S P Romana, J M Lapierre, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|January 14, 2009
A general chemotherapy myelotoxicity score to predict febrile neutropenia in hematological malignanciesM Moreau, J Klastersky, A Schwarzbold, et al.
Clinical Genetics|February 14, 2015
Xq25 duplication: the crucial role of the STAG2 gene in this novel human cohesinopathyC Leroy, M-L Jacquemont, B Doray, et al.
Journal of Medical Genetics|August 6, 2002
Deletion of the SIM1 gene (6q16.2) in a patient with a Prader-Willi-like phenotypeL Faivre, V Cormier-Daire, J M Lapierre, et al.
Journal of Medical Genetics|January 16, 1998
Features of DiGeorge syndrome and CHARGE association in five patientsP de Lonlay-Debeney, V Cormier-Daire, J Amiel, et al.
Pageof 29

Showing results (251-260 of 289) with videos related to

Sort By:
Pageof 29
The Journal of Pediatrics|July 11, 2001
Inversion of the circadian rhythm of melatonin in the Smith-Magenis syndromeH De Leersnyder, M C De Blois, B Claustrat, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|September 28, 2011
[Preimplantation diagnosis with HLA typing: birth of the first double hope child in France]F Lamazou, J Steffann, N Frydman, et al.
Clinical Genetics|October 12, 2001
Comparative genomic hybridisation in mentally retarded patients with dysmorphic features and a normal karyotypeG Joly, J M Lapierre, C Ozilou, et al.
Clinical Genetics|October 16, 2012
Monozygotic twins discordant for submicroscopic chromosomal anomalies in 2p25.3 region detected by array CGHM Rio, G Royer, S Gobin, et al.
Journal of the American Society for Mass Spectrometry|November 14, 2013
False results caused by solvent impurity in tetrahydrofuran for MALDI TOF MS analysis of aminesXianwen Lou, Christianus M A Leenders, Arthur H A M van Onzen, et al.
Clinical Genetics|April 10, 2002
A CGH study of 27 patients with CHARGE associationD Sanlaville, S P Romana, J M Lapierre, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|January 14, 2009
A general chemotherapy myelotoxicity score to predict febrile neutropenia in hematological malignanciesM Moreau, J Klastersky, A Schwarzbold, et al.
Clinical Genetics|February 14, 2015
Xq25 duplication: the crucial role of the STAG2 gene in this novel human cohesinopathyC Leroy, M-L Jacquemont, B Doray, et al.
Journal of Medical Genetics|August 6, 2002
Deletion of the SIM1 gene (6q16.2) in a patient with a Prader-Willi-like phenotypeL Faivre, V Cormier-Daire, J M Lapierre, et al.
Journal of Medical Genetics|January 16, 1998
Features of DiGeorge syndrome and CHARGE association in five patientsP de Lonlay-Debeney, V Cormier-Daire, J Amiel, et al.
Pageof 29