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

M P Roth

Showing results (11-20 of 97) with videos related to

Pageof 10
Sort By:
Journal of Medical Genetics|December 1, 1980
Interstitial deletion of the long arm of chromosome 5 in a deformed boy: 46,XY,del(5)(q13q15)C Stoll, J Levy, M P Roth
Cancer Research|August 1, 1982
Sister chromatid exchange and growth kinetics in chronic myeloid leukemiaC Stoll, F Oberling, M P Roth
Journal De Genetique Humaine|September 1, 1980
[Articular contracture with dwarfism and normal intelligence: a new autosomal dominant familial syndrome]C Stoll, M P Roth, J M Levy
Annales De Genetique|October 20, 1999
Parental consanguinity as a cause for increased incidence of births defects in a study of 238,942 consecutive birthsC Stoll, Y Alembik, M P Roth, et al.
Journal of Medical Genetics|September 1, 1990
Genetic and environmental factors in hypospadiasC Stoll, Y Alembik, M P Roth, et al.
Archives Francaises De Pediatrie|November 1, 1988
[Etiologic and epidemiologic aspects of neural tube defects]C Stoll, B Dott, M P Roth, et al.
Community Genetics|June 5, 2004
Study of 224 cases of oligohydramnios and congenital malformations in a series of 225,669 consecutive birthsC Stoll, Y Alembik, M P Roth, et al.
Genetic Counseling (Geneva, Switzerland)|December 3, 2015
ASSOCIATED NON DIAPHRAGMATIC ANOMALIES AMONG CASES WITH CONGENITAL DIAPHRAGMATIC HERNIAC Stoll, Y Alembik, B Dott, et al.
Archives Francaises De Pediatrie|March 1, 1987
[Congenital malformations in a series of 66,068 consecutive births]M P Roth, B Dott, Y Alembik, et al.
Neuroepidemiology|January 1, 1994
Gender distributions in parents and children concordant for multiple sclerosisM P Roth, J Clayton, E Patois, et al.
Pageof 10

Showing results (11-20 of 97) with videos related to

Sort By:
Pageof 10
Journal of Medical Genetics|December 1, 1980
Interstitial deletion of the long arm of chromosome 5 in a deformed boy: 46,XY,del(5)(q13q15)C Stoll, J Levy, M P Roth
Cancer Research|August 1, 1982
Sister chromatid exchange and growth kinetics in chronic myeloid leukemiaC Stoll, F Oberling, M P Roth
Journal De Genetique Humaine|September 1, 1980
[Articular contracture with dwarfism and normal intelligence: a new autosomal dominant familial syndrome]C Stoll, M P Roth, J M Levy
Annales De Genetique|October 20, 1999
Parental consanguinity as a cause for increased incidence of births defects in a study of 238,942 consecutive birthsC Stoll, Y Alembik, M P Roth, et al.
Journal of Medical Genetics|September 1, 1990
Genetic and environmental factors in hypospadiasC Stoll, Y Alembik, M P Roth, et al.
Archives Francaises De Pediatrie|November 1, 1988
[Etiologic and epidemiologic aspects of neural tube defects]C Stoll, B Dott, M P Roth, et al.
Community Genetics|June 5, 2004
Study of 224 cases of oligohydramnios and congenital malformations in a series of 225,669 consecutive birthsC Stoll, Y Alembik, M P Roth, et al.
Genetic Counseling (Geneva, Switzerland)|December 3, 2015
ASSOCIATED NON DIAPHRAGMATIC ANOMALIES AMONG CASES WITH CONGENITAL DIAPHRAGMATIC HERNIAC Stoll, Y Alembik, B Dott, et al.
Archives Francaises De Pediatrie|March 1, 1987
[Congenital malformations in a series of 66,068 consecutive births]M P Roth, B Dott, Y Alembik, et al.
Neuroepidemiology|January 1, 1994
Gender distributions in parents and children concordant for multiple sclerosisM P Roth, J Clayton, E Patois, et al.
Pageof 10