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

Didier Lacombe

Showing results (11-20 of 309) with videos related to

Pageof 31
Sort By:
American Journal of Medical Genetics. Part A|October 17, 2007
Limb body wall complex and amniotic band sequence in sibsRonaldo Levy, Didier Lacombe, Yannick Rougier, et al.
Genes|July 2, 2021
Rubinstein-Taybi Syndrome: A Model of Epigenetic DisorderJulien Van Gils, Frederique Magdinier, Patricia Fergelot, et al.
American Journal of Medical Genetics|September 24, 2002
Neonatal Proteus syndrome?Atia G Mohamedbhai, A M Hassan Miyan, Didier Lacombe
American Journal of Medical Genetics. Part A|November 11, 2003
Costello syndrome and neurological abnormalitiesMarie-Ange Delrue, Jean-François Chateil, Benoit Arveiler, et al.
Journal of Medical Genetics|February 3, 2022
Oculo-auriculo-vertebral spectrum: new genes and literature review on a complex diseaseAngèle Tingaud-Sequeira, Aurélien Trimouille, Thomas Sagardoy, et al.
Gastroenterologie Clinique Et Biologique|October 31, 2003
Isolated idiopathic chronic pancreatitis associated with a compound heterozygosity for two mutations of the CFTR geneMarie-Pierre Reboul, David Laharie, Michel Amouretti, et al.
International Journal of Molecular Sciences|October 13, 2021
Proteomic Study of Low-Birth-Weight Nephropathy in RatsToshiyuki Imasawa, Stéphane Claverol, Didier Lacombe, et al.
Scientific Reports|December 4, 2018
Prenatal retinoic acid exposure reveals candidate genes for craniofacial disordersMarie Berenguer, Muriel Darnaudery, Stéphane Claverol, et al.
Prenatal Diagnosis|October 15, 2003
Craniofacial dysmorphology and three-dimensional ultrasound: a prospective study on practicability for prenatal diagnosisRaphaele Mangione, Didier Lacombe, Dominique Carles, et al.
Ophthalmic Genetics|November 12, 2010
Keratoconus associated with Williams-Beuren syndrome: first case reportsLoic Pinsard, David Touboul, Yen Vu, et al.
Pageof 31

Showing results (11-20 of 309) with videos related to

Sort By:
Pageof 31
American Journal of Medical Genetics. Part A|October 17, 2007
Limb body wall complex and amniotic band sequence in sibsRonaldo Levy, Didier Lacombe, Yannick Rougier, et al.
Genes|July 2, 2021
Rubinstein-Taybi Syndrome: A Model of Epigenetic DisorderJulien Van Gils, Frederique Magdinier, Patricia Fergelot, et al.
American Journal of Medical Genetics|September 24, 2002
Neonatal Proteus syndrome?Atia G Mohamedbhai, A M Hassan Miyan, Didier Lacombe
American Journal of Medical Genetics. Part A|November 11, 2003
Costello syndrome and neurological abnormalitiesMarie-Ange Delrue, Jean-François Chateil, Benoit Arveiler, et al.
Journal of Medical Genetics|February 3, 2022
Oculo-auriculo-vertebral spectrum: new genes and literature review on a complex diseaseAngèle Tingaud-Sequeira, Aurélien Trimouille, Thomas Sagardoy, et al.
Gastroenterologie Clinique Et Biologique|October 31, 2003
Isolated idiopathic chronic pancreatitis associated with a compound heterozygosity for two mutations of the CFTR geneMarie-Pierre Reboul, David Laharie, Michel Amouretti, et al.
International Journal of Molecular Sciences|October 13, 2021
Proteomic Study of Low-Birth-Weight Nephropathy in RatsToshiyuki Imasawa, Stéphane Claverol, Didier Lacombe, et al.
Scientific Reports|December 4, 2018
Prenatal retinoic acid exposure reveals candidate genes for craniofacial disordersMarie Berenguer, Muriel Darnaudery, Stéphane Claverol, et al.
Prenatal Diagnosis|October 15, 2003
Craniofacial dysmorphology and three-dimensional ultrasound: a prospective study on practicability for prenatal diagnosisRaphaele Mangione, Didier Lacombe, Dominique Carles, et al.
Ophthalmic Genetics|November 12, 2010
Keratoconus associated with Williams-Beuren syndrome: first case reportsLoic Pinsard, David Touboul, Yen Vu, et al.
Pageof 31