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

S Odent

Showing results (21-30 of 110) with videos related to

Pageof 11
Sort By:
Journal De Genetique Humaine|September 1, 1989
[Truncus arteriosus: an autosomal recessive disease?]B le Marec, S Odent, C Almange, et al.
Revue Francaise De Gynecologie Et D'Obstetrique|July 1, 1991
[Therapeutic termination of pregnancy. Diagnosis and protocols. 54 cases]D Berger, S Odent, J Lévêque, et al.
Prenatal Diagnosis|March 1, 1997
Prenatal detection of a congenital pancreatic cyst and Beckwith-Wiedemann syndromeB Fremond, P Poulain, S Odent, et al.
Human Genetics|December 1, 1991
Oto-palato-digital syndrome type I: further evidence for assignment of the locus to Xq28V Biancalana, B Le Marec, S Odent, et al.
Pediatrie|January 1, 1993
[Rapid diagnosis of tuberculous meningitis by polymerase chain reaction. A case in an infant]S Odent, J Minet, R Lelièvre, et al.
Human Mutation|March 27, 1999
Identification of three novel mutations in the dystrophin gene detected by the heteroduplex/SSCA screening procedure. Mutations in brief no. 222. OnlineC Dubourg, S Odent, P Fergelot, et al.
Clinical Genetics|August 1, 1988
Genetic counselling in a case of TAR syndrome where the father presented malformations of the feetB Le Marec, S Odent, H Bracq, et al.
Annales De Genetique|January 1, 1988
[Oto-palato-digital type I syndrome in five generations. Relationship to the type II form]B Le Marec, S Odent, E Bracq, et al.
European Journal of Human Genetics : EJHG|October 20, 2000
A new mutation in the six-domain of SIX3 gene causes holoprosencephalyL Pasquier, C Dubourg, M Blayau, et al.
Journal of Medical Genetics|January 7, 2005
First occurrence of aprosencephaly/atelencephaly and holoprosencephaly in a family with a SIX3 gene mutation and phenotype/genotype correlation in our series of SIX3 mutationsL Pasquier, C Dubourg, M Gonzales, et al.
Pageof 11

Showing results (21-30 of 110) with videos related to

Sort By:
Pageof 11
Journal De Genetique Humaine|September 1, 1989
[Truncus arteriosus: an autosomal recessive disease?]B le Marec, S Odent, C Almange, et al.
Revue Francaise De Gynecologie Et D'Obstetrique|July 1, 1991
[Therapeutic termination of pregnancy. Diagnosis and protocols. 54 cases]D Berger, S Odent, J Lévêque, et al.
Prenatal Diagnosis|March 1, 1997
Prenatal detection of a congenital pancreatic cyst and Beckwith-Wiedemann syndromeB Fremond, P Poulain, S Odent, et al.
Human Genetics|December 1, 1991
Oto-palato-digital syndrome type I: further evidence for assignment of the locus to Xq28V Biancalana, B Le Marec, S Odent, et al.
Pediatrie|January 1, 1993
[Rapid diagnosis of tuberculous meningitis by polymerase chain reaction. A case in an infant]S Odent, J Minet, R Lelièvre, et al.
Human Mutation|March 27, 1999
Identification of three novel mutations in the dystrophin gene detected by the heteroduplex/SSCA screening procedure. Mutations in brief no. 222. OnlineC Dubourg, S Odent, P Fergelot, et al.
Clinical Genetics|August 1, 1988
Genetic counselling in a case of TAR syndrome where the father presented malformations of the feetB Le Marec, S Odent, H Bracq, et al.
Annales De Genetique|January 1, 1988
[Oto-palato-digital type I syndrome in five generations. Relationship to the type II form]B Le Marec, S Odent, E Bracq, et al.
European Journal of Human Genetics : EJHG|October 20, 2000
A new mutation in the six-domain of SIX3 gene causes holoprosencephalyL Pasquier, C Dubourg, M Blayau, et al.
Journal of Medical Genetics|January 7, 2005
First occurrence of aprosencephaly/atelencephaly and holoprosencephaly in a family with a SIX3 gene mutation and phenotype/genotype correlation in our series of SIX3 mutationsL Pasquier, C Dubourg, M Gonzales, et al.
Pageof 11