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

A Raas-Rothschild

Showing results (1-10 of 36) with videos related to

Pageof 4
Sort By:
American Journal of Medical Genetics|January 1, 1988
Megalocornea and mental retardation syndromeA Raas-Rothschild, M Berkenstadt, R M Goodman
American Journal of Medical Genetics|March 4, 2000
Giant congenital aortic aneurysm with cleft sternum, supraumbilical raphé, and hemangiomatosis: report and reviewA Raas-Rothschild, A Nir, R Gillis, et al.
Clinical Genetics|August 1, 1990
Megalocornea, macrocephaly, mental and motor retardation (MMMM)M Frydman, M Berkenstadt, A Raas-Rothschild, et al.
Biochemical Medicine and Metabolic Biology|June 1, 1994
Mutations of the hexosaminidase A gene in Ashkenazi and non-Ashkenazi JewsL Peleg, M Karpati, E Gazit, et al.
The Journal of Pediatrics|July 1, 1991
Ambulatory intravenous therapy for chronic suppurative otitis mediaA Raas-Rothschild, R Lang, A Schabtai, et al.
European Journal of Human Genetics : EJHG|June 3, 1999
Mucolipidosis type IV: the origin of the disease in the Ashkenazi Jewish populationA Raas-Rothschild, R Bargal, S DellaPergola, et al.
Dermatologica|January 1, 1990
Subcutaneous fat necrosis with thrombocytopenia in a newborn infantB Wolach, A Raas-Rothschild, R Vogel, et al.
Journal of Craniofacial Genetics and Developmental Biology|January 1, 1988
Klippel-Feil anomaly with sacral agenesis: an additional subtype, type IVA Raas-Rothschild, R M Goodman, M Grunbaum, et al.
Pediatric Cardiology|March 15, 2002
Rhabdomyoma in the fetus: illustration of tumor growth during the second half of gestationA Nir, S Ekstein, M Nadjari, et al.
American Journal of Human Genetics|October 30, 1998
Prenatal diagnosis and carrier detection for a point mutation in UBE3A causing Angelman syndromeT F Tsai, A Raas-Rothschild, Z Ben-Neriah, et al.
Pageof 4

Showing results (1-10 of 36) with videos related to

Sort By:
Pageof 4
American Journal of Medical Genetics|January 1, 1988
Megalocornea and mental retardation syndromeA Raas-Rothschild, M Berkenstadt, R M Goodman
American Journal of Medical Genetics|March 4, 2000
Giant congenital aortic aneurysm with cleft sternum, supraumbilical raphé, and hemangiomatosis: report and reviewA Raas-Rothschild, A Nir, R Gillis, et al.
Clinical Genetics|August 1, 1990
Megalocornea, macrocephaly, mental and motor retardation (MMMM)M Frydman, M Berkenstadt, A Raas-Rothschild, et al.
Biochemical Medicine and Metabolic Biology|June 1, 1994
Mutations of the hexosaminidase A gene in Ashkenazi and non-Ashkenazi JewsL Peleg, M Karpati, E Gazit, et al.
The Journal of Pediatrics|July 1, 1991
Ambulatory intravenous therapy for chronic suppurative otitis mediaA Raas-Rothschild, R Lang, A Schabtai, et al.
European Journal of Human Genetics : EJHG|June 3, 1999
Mucolipidosis type IV: the origin of the disease in the Ashkenazi Jewish populationA Raas-Rothschild, R Bargal, S DellaPergola, et al.
Dermatologica|January 1, 1990
Subcutaneous fat necrosis with thrombocytopenia in a newborn infantB Wolach, A Raas-Rothschild, R Vogel, et al.
Journal of Craniofacial Genetics and Developmental Biology|January 1, 1988
Klippel-Feil anomaly with sacral agenesis: an additional subtype, type IVA Raas-Rothschild, R M Goodman, M Grunbaum, et al.
Pediatric Cardiology|March 15, 2002
Rhabdomyoma in the fetus: illustration of tumor growth during the second half of gestationA Nir, S Ekstein, M Nadjari, et al.
American Journal of Human Genetics|October 30, 1998
Prenatal diagnosis and carrier detection for a point mutation in UBE3A causing Angelman syndromeT F Tsai, A Raas-Rothschild, Z Ben-Neriah, et al.
Pageof 4