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

N B Spinner

Showing results (1-10 of 63) with videos related to

Pageof 7
Sort By:
The Journal of Clinical Investigation|March 11, 2000
CADASIL: Notch signaling defect or protein accumulation problem?N B Spinner
Gastroenterology|April 30, 1999
Alagille syndrome and the notch signaling pathway: new insights into human developmentN B Spinner
Seminars in Liver Disease|December 18, 2001
Alagille syndrome and the Jagged1 geneD A Piccoli, N B Spinner
American Journal of Human Genetics|February 1, 1986
Polymorphisms of mitochondrially encoded proteinsN B Spinner, M C King
American Journal of Medical Genetics|April 1, 1992
Frequency of the common fragile site at Xq27.2 under conditions of thymidylate stress: implications for cytogenetic diagnosis of the fragile-X syndromeF J Ramos, B S Emanuel, N B Spinner
Clinical Genetics|January 1, 1991
Recurrent neuroleptic malignant syndrome associated with inv dup(15) and mental retardationA L Lazarus, K E Moore, N B Spinner
Human Molecular Genetics|February 7, 2001
Defective intracellular transport and processing of JAG1 missense mutations in Alagille syndromeJ D Morrissette, R P Colliton, N B Spinner
Journal of Medical Genetics|February 1, 1997
Alagille syndromeI D Krantz, D A Piccoli, N B Spinner
Current Opinion in Pediatrics|December 11, 1999
Clinical and molecular genetics of Alagille syndromeI D Krantz, D A Piccoli, N B Spinner
American Journal of Medical Genetics|April 1, 1991
Holoprosencephaly in a newborn girl with 46,XX,i(18q)N B Spinner, D L Eunpu, J R Austria, et al.
Pageof 7

Showing results (1-10 of 63) with videos related to

Sort By:
Pageof 7
The Journal of Clinical Investigation|March 11, 2000
CADASIL: Notch signaling defect or protein accumulation problem?N B Spinner
Gastroenterology|April 30, 1999
Alagille syndrome and the notch signaling pathway: new insights into human developmentN B Spinner
Seminars in Liver Disease|December 18, 2001
Alagille syndrome and the Jagged1 geneD A Piccoli, N B Spinner
American Journal of Human Genetics|February 1, 1986
Polymorphisms of mitochondrially encoded proteinsN B Spinner, M C King
American Journal of Medical Genetics|April 1, 1992
Frequency of the common fragile site at Xq27.2 under conditions of thymidylate stress: implications for cytogenetic diagnosis of the fragile-X syndromeF J Ramos, B S Emanuel, N B Spinner
Clinical Genetics|January 1, 1991
Recurrent neuroleptic malignant syndrome associated with inv dup(15) and mental retardationA L Lazarus, K E Moore, N B Spinner
Human Molecular Genetics|February 7, 2001
Defective intracellular transport and processing of JAG1 missense mutations in Alagille syndromeJ D Morrissette, R P Colliton, N B Spinner
Journal of Medical Genetics|February 1, 1997
Alagille syndromeI D Krantz, D A Piccoli, N B Spinner
Current Opinion in Pediatrics|December 11, 1999
Clinical and molecular genetics of Alagille syndromeI D Krantz, D A Piccoli, N B Spinner
American Journal of Medical Genetics|April 1, 1991
Holoprosencephaly in a newborn girl with 46,XX,i(18q)N B Spinner, D L Eunpu, J R Austria, et al.
Pageof 7