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

G J Bargman

Showing results (11-20 of 21) with videos related to

Pageof 3
Sort By:
Archives of Biochemistry and Biophysics|October 1, 1973
Studies of mitochondrial energy systems during embryogenesis in the ratB Mackler, R Grace, B Haynes, et al.
The Journal of Pediatrics|April 1, 1979
Lack of inhibition of vasopressin release in midfacial hypoplasiaA L Friedman, R W Chesney, G J Bargman, et al.
Journal of Medical Genetics|March 1, 1970
A 46,XX,t(Cp+;Cq-) translocation in a girl with multiple congenital anomalies and in her phenotypically normal father 46,XY,t(Cq+;Cq-)G J Bargman, R L Neu, H O Powers, et al.
European Journal of Pediatrics|March 18, 1977
Absence of spermatogonia in the Prader-Willi syndromeM L Katcher, G J Bargman, E F Gilbert, et al.
Journal of Medical Genetics|March 1, 1970
48,XY,21+, mar+mat: a case of trisomy 21 associated with an inherited small marker chromosomeG J Bargman, R L Neu, H O Powers, et al.
Clinical Nuclear Medicine|July 1, 1981
Adrenal scan in 17-alpha-hydroxylase deficiency: false indication of adrenal adenomaR M Shore, L M Lieberman, T J Newman, et al.
Archives of Pathology & Laboratory Medicine|April 1, 1977
Sudden infant death due to congenital adrenal hypoplasiaM A Russell, J M Opitz, C Viseskul, et al.
Family Process|December 1, 1981
Anorexia Nervosa: the hospital's role in family treatmentS Stern, C A Whitaker, N J Hagemann, et al.
Calcified Tissue International|January 1, 1982
Skeletal demineralization in Turner's syndromeR M Shore, R W Chesney, R B Mazess, et al.
Calcified Tissue International|January 1, 1981
Osteopenia in juvenile diabetesR M Shore, R W Chesney, R B Mazess, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Archives of Biochemistry and Biophysics|October 1, 1973
Studies of mitochondrial energy systems during embryogenesis in the ratB Mackler, R Grace, B Haynes, et al.
The Journal of Pediatrics|April 1, 1979
Lack of inhibition of vasopressin release in midfacial hypoplasiaA L Friedman, R W Chesney, G J Bargman, et al.
Journal of Medical Genetics|March 1, 1970
A 46,XX,t(Cp+;Cq-) translocation in a girl with multiple congenital anomalies and in her phenotypically normal father 46,XY,t(Cq+;Cq-)G J Bargman, R L Neu, H O Powers, et al.
European Journal of Pediatrics|March 18, 1977
Absence of spermatogonia in the Prader-Willi syndromeM L Katcher, G J Bargman, E F Gilbert, et al.
Journal of Medical Genetics|March 1, 1970
48,XY,21+, mar+mat: a case of trisomy 21 associated with an inherited small marker chromosomeG J Bargman, R L Neu, H O Powers, et al.
Clinical Nuclear Medicine|July 1, 1981
Adrenal scan in 17-alpha-hydroxylase deficiency: false indication of adrenal adenomaR M Shore, L M Lieberman, T J Newman, et al.
Archives of Pathology & Laboratory Medicine|April 1, 1977
Sudden infant death due to congenital adrenal hypoplasiaM A Russell, J M Opitz, C Viseskul, et al.
Family Process|December 1, 1981
Anorexia Nervosa: the hospital's role in family treatmentS Stern, C A Whitaker, N J Hagemann, et al.
Calcified Tissue International|January 1, 1982
Skeletal demineralization in Turner's syndromeR M Shore, R W Chesney, R B Mazess, et al.
Calcified Tissue International|January 1, 1981
Osteopenia in juvenile diabetesR M Shore, R W Chesney, R B Mazess, et al.
Pageof 3