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

R Carmi

Showing results (41-50 of 103) with videos related to

Pageof 11
Sort By:
Journal of Natural Products|September 1, 1994
(+)-(S)-dihydroaeruginoic acid, an inhibitor of Septoria tritici and other phytopathogenic fungi and bacteria, produced by Pseudomonas fluorescensR Carmi, S Carmeli, E Levy, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Characterization of the mutations in the glucose-6-phosphatase gene in Israeli patients with glycogen storage disease type 1a: R83C in six Jews and a novel V166G mutation in a Muslim ArabR Parvari, S Moses, E Hershkovitz, et al.
American Journal of Medical Genetics|February 15, 1994
Linkage localization of the thoraco-abdominal syndrome (TAS) gene to Xq25-26R Parvari, Y Weinstein, S Ehrlich, et al.
American Journal of Medical Genetics|August 15, 1994
Cardiac abnormalities in the Bardet-Biedl syndrome: echocardiographic studies of 22 patientsK Elbedour, N Zucker, E Zalzstein, et al.
American Journal of Medical Genetics|November 6, 1995
Phenotypic differences among patients with Bardet-Biedl syndrome linked to three different chromosome lociR Carmi, K Elbedour, E M Stone, et al.
Birth Defects Original Article Series|January 1, 1996
Mapping of an X-linked gene for ventral midline defects (the TAS gene)R Carmi, R Parvari, S Ehrlich, et al.
Pediatrics|November 1, 1984
Fragile-X syndrome ascertained by the presence of macro-orchidism in a 5-month-old infantR Carmi, D L Meryash, J Wood, et al.
Birth Defects Original Article Series|January 1, 1982
Hirschsprung disease in progeny of affected individuals: a case report and review of the literatureR Carmi, P Hawley, J W Wood, et al.
American Journal of Medical Genetics|December 1, 1990
Persistent hyperinsulinemic hypoglycemia of infancy ("nesidioblastosis"): autosomal recessive inheritance in 7 pedigreesB Glaser, M Phillip, R Carmi, et al.
The British Journal of Dermatology|September 25, 1998
Reticulolinear aplasia cutis congenita of the face and neck: a distinctive cutaneous manifestation in several syndromes linked to Xp22A Zvulunov, L Kachko, E Manor, et al.
Pageof 11

Showing results (41-50 of 103) with videos related to

Sort By:
Pageof 11
Journal of Natural Products|September 1, 1994
(+)-(S)-dihydroaeruginoic acid, an inhibitor of Septoria tritici and other phytopathogenic fungi and bacteria, produced by Pseudomonas fluorescensR Carmi, S Carmeli, E Levy, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Characterization of the mutations in the glucose-6-phosphatase gene in Israeli patients with glycogen storage disease type 1a: R83C in six Jews and a novel V166G mutation in a Muslim ArabR Parvari, S Moses, E Hershkovitz, et al.
American Journal of Medical Genetics|February 15, 1994
Linkage localization of the thoraco-abdominal syndrome (TAS) gene to Xq25-26R Parvari, Y Weinstein, S Ehrlich, et al.
American Journal of Medical Genetics|August 15, 1994
Cardiac abnormalities in the Bardet-Biedl syndrome: echocardiographic studies of 22 patientsK Elbedour, N Zucker, E Zalzstein, et al.
American Journal of Medical Genetics|November 6, 1995
Phenotypic differences among patients with Bardet-Biedl syndrome linked to three different chromosome lociR Carmi, K Elbedour, E M Stone, et al.
Birth Defects Original Article Series|January 1, 1996
Mapping of an X-linked gene for ventral midline defects (the TAS gene)R Carmi, R Parvari, S Ehrlich, et al.
Pediatrics|November 1, 1984
Fragile-X syndrome ascertained by the presence of macro-orchidism in a 5-month-old infantR Carmi, D L Meryash, J Wood, et al.
Birth Defects Original Article Series|January 1, 1982
Hirschsprung disease in progeny of affected individuals: a case report and review of the literatureR Carmi, P Hawley, J W Wood, et al.
American Journal of Medical Genetics|December 1, 1990
Persistent hyperinsulinemic hypoglycemia of infancy ("nesidioblastosis"): autosomal recessive inheritance in 7 pedigreesB Glaser, M Phillip, R Carmi, et al.
The British Journal of Dermatology|September 25, 1998
Reticulolinear aplasia cutis congenita of the face and neck: a distinctive cutaneous manifestation in several syndromes linked to Xp22A Zvulunov, L Kachko, E Manor, et al.
Pageof 11