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 (221-230 of 377) with videos related to

Pageof 38
Sort By:
La Nouvelle Presse Medicale|February 5, 1972
[Transient neonatal thrombopenia of trisomy 21]C Stoll, R Sacrez, D Willard, et al.
Prenatal Diagnosis|January 1, 1991
Prenatal diagnosis of congenital myasthenia with arthrogryposis in a myasthenic motherC Stoll, M C Ehret-Mentre, A Treisser, et al.
Journal of Medical Genetics|February 1, 1979
Abnormal children of a 47,XYY fatherC Stoll, E Flori, A Clavert, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1992
Tau syndrome (thrombocytopenia and absent ulnar) with mental retardation and facial dysmorphyC Stoll, S Finck, B Janser, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|February 1, 1997
[Anomalies of thyroid function in children with Down syndrome]C Toledo, Y Alembik, B Dott, et al.
Prenatal Diagnosis|April 1, 1994
Hepatic calcifications in a fetus with trisomy 9 that underwent cordocentesisD Satge, B Gasser, A Geneix, et al.
Pediatrie|July 1, 1980
[Familial mitochondrial myopathy with eczema and mental retardation]C Stoll, M Fischbach, P R Walter, et al.
Revue Francaise De Gynecologie Et D'Obstetrique|January 1, 1990
[Oligo-elements of the amniotic fluid from normal, hypotrophic and trisomy 21 fetuses]C Stoll, B Dott, E A Maier, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1993
Twelve cases with hemihypertrophy: etiology and follow upC Stoll, Y Alembik, J P Steib, et al.
American Journal of Medical Genetics|February 1, 1985
Male-to-male transmission of the hypertelorism-hypospadias (BBB) syndromeC Stoll, A Geraudel, H Berland, et al.
Pageof 38

Showing results (221-230 of 377) with videos related to

Sort By:
Pageof 38
La Nouvelle Presse Medicale|February 5, 1972
[Transient neonatal thrombopenia of trisomy 21]C Stoll, R Sacrez, D Willard, et al.
Prenatal Diagnosis|January 1, 1991
Prenatal diagnosis of congenital myasthenia with arthrogryposis in a myasthenic motherC Stoll, M C Ehret-Mentre, A Treisser, et al.
Journal of Medical Genetics|February 1, 1979
Abnormal children of a 47,XYY fatherC Stoll, E Flori, A Clavert, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1992
Tau syndrome (thrombocytopenia and absent ulnar) with mental retardation and facial dysmorphyC Stoll, S Finck, B Janser, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|February 1, 1997
[Anomalies of thyroid function in children with Down syndrome]C Toledo, Y Alembik, B Dott, et al.
Prenatal Diagnosis|April 1, 1994
Hepatic calcifications in a fetus with trisomy 9 that underwent cordocentesisD Satge, B Gasser, A Geneix, et al.
Pediatrie|July 1, 1980
[Familial mitochondrial myopathy with eczema and mental retardation]C Stoll, M Fischbach, P R Walter, et al.
Revue Francaise De Gynecologie Et D'Obstetrique|January 1, 1990
[Oligo-elements of the amniotic fluid from normal, hypotrophic and trisomy 21 fetuses]C Stoll, B Dott, E A Maier, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1993
Twelve cases with hemihypertrophy: etiology and follow upC Stoll, Y Alembik, J P Steib, et al.
American Journal of Medical Genetics|February 1, 1985
Male-to-male transmission of the hypertelorism-hypospadias (BBB) syndromeC Stoll, A Geraudel, H Berland, et al.
Pageof 38