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 Stoll

Showing results (211-220 of 377) with videos related to

Pageof 38
Sort By:
Clinical Genetics|November 1, 1980
Familial pterygium syndromeC Stoll, J M Levy, P Kehr, et al.
Pediatrie|March 1, 1974
[Chromosome abnormalities in Fanconi's anemia. Apropos of 4 cases]C Stoll, J G Juif, J M Lévy, et al.
Pediatrie|June 1, 1979
[Combined effects of ethanol and antiepileptics on the fetus. Apropos of 2 cases]J J Kuss, M Fischbach, C Stoll, et al.
Genetic Counseling (Geneva, Switzerland)|October 28, 2003
Multiple congenital malformations including generalized hypertrichosis with gum hypertrophy in a child exposed to valproic acid in uteroC Stoll, F Audeoud, C Gaugler, et al.
Environmental Science & Technology|August 1, 2012
Prevalence of clinically relevant antibiotic resistance genes in surface water samples collected from Germany and AustraliaC Stoll, J P S Sidhu, A Tiehm, et al.
Journal De Genetique Humaine|December 1, 1974
[Genetic study of familial blepharophimosis (autosome dominant disease)]C Stoll, J M Levy, P Bigel, et al.
American Journal of Medical Genetics|September 1, 1990
Dandy-Walker variant malformation, spastic paraplegia, and mental retardation in two sibsC Stoll, C Huber, Y Alembik, et al.
Archives Francaises De Pediatrie|October 1, 1993
[The MASA syndrome (Mental retardation, Aphasia, Spastic paraplegia and Adducted thumbs), is it heterogeneous?]C Stoll, Y Alembik, M Pfindel, et al.
Humangenetik|January 1, 1975
Ring chromosome 15:r(15). Identification by R bandingC Stoll, J G Juif, J C Luckel, et al.
Annales De Pediatrie|September 1, 1988
[Coffin-Siris syndrome with Lennox-Gastaut syndrome and hypertrophic cardiomyopathy]Y Alembik, E Roy, E Hirsch, et al.
Pageof 38

Showing results (211-220 of 377) with videos related to

Sort By:
Pageof 38
Clinical Genetics|November 1, 1980
Familial pterygium syndromeC Stoll, J M Levy, P Kehr, et al.
Pediatrie|March 1, 1974
[Chromosome abnormalities in Fanconi's anemia. Apropos of 4 cases]C Stoll, J G Juif, J M Lévy, et al.
Pediatrie|June 1, 1979
[Combined effects of ethanol and antiepileptics on the fetus. Apropos of 2 cases]J J Kuss, M Fischbach, C Stoll, et al.
Genetic Counseling (Geneva, Switzerland)|October 28, 2003
Multiple congenital malformations including generalized hypertrichosis with gum hypertrophy in a child exposed to valproic acid in uteroC Stoll, F Audeoud, C Gaugler, et al.
Environmental Science & Technology|August 1, 2012
Prevalence of clinically relevant antibiotic resistance genes in surface water samples collected from Germany and AustraliaC Stoll, J P S Sidhu, A Tiehm, et al.
Journal De Genetique Humaine|December 1, 1974
[Genetic study of familial blepharophimosis (autosome dominant disease)]C Stoll, J M Levy, P Bigel, et al.
American Journal of Medical Genetics|September 1, 1990
Dandy-Walker variant malformation, spastic paraplegia, and mental retardation in two sibsC Stoll, C Huber, Y Alembik, et al.
Archives Francaises De Pediatrie|October 1, 1993
[The MASA syndrome (Mental retardation, Aphasia, Spastic paraplegia and Adducted thumbs), is it heterogeneous?]C Stoll, Y Alembik, M Pfindel, et al.
Humangenetik|January 1, 1975
Ring chromosome 15:r(15). Identification by R bandingC Stoll, J G Juif, J C Luckel, et al.
Annales De Pediatrie|September 1, 1988
[Coffin-Siris syndrome with Lennox-Gastaut syndrome and hypertrophic cardiomyopathy]Y Alembik, E Roy, E Hirsch, et al.
Pageof 38