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 Manouvrier

Showing results (21-30 of 79) with videos related to

Pageof 8
Sort By:
Prenatal Diagnosis|November 1, 1992
First-trimester prenatal exclusion of PIBIDS syndrome with normal DNA excision repair on chorionic villus cellsJ B Savary, F Vasseur, D Vinatier, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|August 30, 2001
[Dyggve-Melchior-Clausen syndrome: differential diagnosis of mucopolysaccharidosis type IV or Morquio disease]A Coëslier, O Boute-Bénéjean, A Moerman, et al.
American Journal of Medical Genetics|March 1, 1987
The GAPO syndromeS Manouvrier-Hanu, C Largilliere, M Benalioua, et al.
American Journal of Medical Genetics|March 8, 2000
Radioulnar synostosis, radial ray abnormalities, and severe malformations in the male: a new X-linked dominant multiple congenital anomalies syndrome?S Manouvrier, A Moerman, A Coeslier, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1996
Fryns syndrome and erupted teeth in a 24-weeks-old fetusS Manouvrier-Hanu, L Devisme, P Vaast, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|August 28, 2001
Pure ectodermal dysplasia: retrospective study of 16 cases and literature reviewB Ruhin, V Martinot, P Lafforgue, et al.
Pediatrie|January 1, 1988
[Stickler's syndrome or hereditary progressive arthro-ophthalmopathy]A C De la Chapelle, S Manouvrier, J P Dubos, et al.
American Journal of Medical Genetics|December 14, 1999
The Richieri-Costa and Pereira form of acrofacial dysostosis: first case in a non-Brazilian infantE Walter-Nicolet, A Coëslier, S Joriot, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|May 16, 1998
[Prenatal diagnosis of osteogenesis imperfecta. Two cases]I Baalbaky, S Manouvrier, P Dufour, et al.
Journal of Medical Genetics|April 16, 1998
Extensive germinal mosaicism in a family with X linked myotubular myopathy simulates genetic heterogeneityM C Vincent, C Guiraud-Chaumeil, J Laporte, et al.
Pageof 8

Showing results (21-30 of 79) with videos related to

Sort By:
Pageof 8
Prenatal Diagnosis|November 1, 1992
First-trimester prenatal exclusion of PIBIDS syndrome with normal DNA excision repair on chorionic villus cellsJ B Savary, F Vasseur, D Vinatier, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|August 30, 2001
[Dyggve-Melchior-Clausen syndrome: differential diagnosis of mucopolysaccharidosis type IV or Morquio disease]A Coëslier, O Boute-Bénéjean, A Moerman, et al.
American Journal of Medical Genetics|March 1, 1987
The GAPO syndromeS Manouvrier-Hanu, C Largilliere, M Benalioua, et al.
American Journal of Medical Genetics|March 8, 2000
Radioulnar synostosis, radial ray abnormalities, and severe malformations in the male: a new X-linked dominant multiple congenital anomalies syndrome?S Manouvrier, A Moerman, A Coeslier, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1996
Fryns syndrome and erupted teeth in a 24-weeks-old fetusS Manouvrier-Hanu, L Devisme, P Vaast, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|August 28, 2001
Pure ectodermal dysplasia: retrospective study of 16 cases and literature reviewB Ruhin, V Martinot, P Lafforgue, et al.
Pediatrie|January 1, 1988
[Stickler's syndrome or hereditary progressive arthro-ophthalmopathy]A C De la Chapelle, S Manouvrier, J P Dubos, et al.
American Journal of Medical Genetics|December 14, 1999
The Richieri-Costa and Pereira form of acrofacial dysostosis: first case in a non-Brazilian infantE Walter-Nicolet, A Coëslier, S Joriot, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|May 16, 1998
[Prenatal diagnosis of osteogenesis imperfecta. Two cases]I Baalbaky, S Manouvrier, P Dufour, et al.
Journal of Medical Genetics|April 16, 1998
Extensive germinal mosaicism in a family with X linked myotubular myopathy simulates genetic heterogeneityM C Vincent, C Guiraud-Chaumeil, J Laporte, et al.
Pageof 8