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

C Francannet

Showing results (11-20 of 48) with videos related to

Pageof 5
Sort By:
Journal De Genetique Humaine|December 1, 1989
[Renal agenesis and the Fraser syndrome: 4 observations]P Vanlieferinghen, C Francannet, E Robert, et al.
European Journal of Epidemiology|November 1, 1993
The epidemiology of three serious cardiac defects. A joint study between five centresC Francannet, P A Lancaster, P Pradat, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|August 14, 2012
[Macrocephaly-capillary malformation. A neonatal case]K Coste, C Sarret, A Cisse, et al.
American Journal of Medical Genetics|August 1, 1990
Fraser syndrome with renal agenesis in two consanguineous Turkish familiesC Francannet, P Lefrançois, P Dechelotte, et al.
Journal De Genetique Humaine|December 1, 1989
[Diagnosis of deficiency in cofactor of phenylalanine hydroxylase: a metabolic emergency]M Meyer, G Malpuech, J Geneste, et al.
Journal De Genetique Humaine|August 1, 1987
[Value of muscle studies in the early diagnosis of Schwartz-Jampel syndrome]P Vanlieferighen, C Francannet, P Dechelotte, et al.
American Journal of Medical Genetics|March 21, 1998
X-linked mental retardation with isolated growth hormone deficiency is mapped to Xq22-Xq27.2 in one familyM Raynaud, N Ronce, A D Ayrault, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1994
LADD syndrome in five members of a three-generation family and prenatal diagnosisC Francannet, P Vanlieferinghen, P Dechelotte, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|October 1, 2019
Prenatal diagnosis of hemimegalencephaly revealing tuberous sclerosis complexS Bruet, C Francannet, F Marguet, et al.
Prenatal Diagnosis|August 1, 1993
Prenatal diagnosis of spina bifida aperta after first-trimester valproate exposureS Guibaud, E Robert, A Simplot, et al.
Pageof 5

Showing results (11-20 of 48) with videos related to

Sort By:
Pageof 5
Journal De Genetique Humaine|December 1, 1989
[Renal agenesis and the Fraser syndrome: 4 observations]P Vanlieferinghen, C Francannet, E Robert, et al.
European Journal of Epidemiology|November 1, 1993
The epidemiology of three serious cardiac defects. A joint study between five centresC Francannet, P A Lancaster, P Pradat, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|August 14, 2012
[Macrocephaly-capillary malformation. A neonatal case]K Coste, C Sarret, A Cisse, et al.
American Journal of Medical Genetics|August 1, 1990
Fraser syndrome with renal agenesis in two consanguineous Turkish familiesC Francannet, P Lefrançois, P Dechelotte, et al.
Journal De Genetique Humaine|December 1, 1989
[Diagnosis of deficiency in cofactor of phenylalanine hydroxylase: a metabolic emergency]M Meyer, G Malpuech, J Geneste, et al.
Journal De Genetique Humaine|August 1, 1987
[Value of muscle studies in the early diagnosis of Schwartz-Jampel syndrome]P Vanlieferighen, C Francannet, P Dechelotte, et al.
American Journal of Medical Genetics|March 21, 1998
X-linked mental retardation with isolated growth hormone deficiency is mapped to Xq22-Xq27.2 in one familyM Raynaud, N Ronce, A D Ayrault, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1994
LADD syndrome in five members of a three-generation family and prenatal diagnosisC Francannet, P Vanlieferinghen, P Dechelotte, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|October 1, 2019
Prenatal diagnosis of hemimegalencephaly revealing tuberous sclerosis complexS Bruet, C Francannet, F Marguet, et al.
Prenatal Diagnosis|August 1, 1993
Prenatal diagnosis of spina bifida aperta after first-trimester valproate exposureS Guibaud, E Robert, A Simplot, et al.
Pageof 5