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 (11-20 of 36) with videos related to

Pageof 4
Sort By:
American Journal of Medical Genetics|November 14, 2000
Contribution of connexin 26 mutations to nonsyndromic deafness in Ashkenazi patients and the variable phenotypic effect of the mutation 167delTI Lerer, M Sagi, E Malamud, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|January 16, 2003
Prenatal ultrasonographic diagnosis of atypical Nonne-Milroy lymphedemaA Lev-Sagie, Y Hamani, A Raas-Rothschild, et al.
American Journal of Medical Genetics|May 26, 1999
Agenesis of tibia with ectrodactyly/Gollop-Wolfgang complex associated with congenital heart malformations and additional skeletal abnormalitiesA Raas-Rothschild, A Nir, Z Ergaz, et al.
American Journal of Human Genetics|June 1, 1993
Negative expansion of the myotonic dystrophy unstable sequenceD Abeliovich, I Lerer, I Pashut-Lavon, et al.
Journal of Medical Genetics|December 1, 1996
Refined mapping of a gene for split hand-split foot malformation (SHFM3) on chromosome 10q25A Raas-Rothschild, S Manouvrier, M Gonzales, et al.
British Journal of Nursing (Mark Allen Publishing)|June 20, 2008
Home-based infusion therapy for patients with Fabry diseaseA Cousins, P Lee, D Rorman, et al.
The Pediatric Infectious Disease Journal|November 1, 1992
Oral ciprofloxacin in the management of chronic suppurative otitis media without cholesteatoma in children: preliminary experience in 21 childrenR Lang, S Goshen, A Raas-Rothschild, et al.
Prenatal Diagnosis|August 22, 2000
Ultrasonographic prenatal diagnosis of microcephalic osteodysplastic primordial dwarfism types I/IIIM Nadjari, S J Fasouliotis, I Ariel, et al.
Prenatal Diagnosis|March 11, 2003
Mucolipidosis III type C: first-trimester biochemical and molecular prenatal diagnosisT C Falik-Zaccai, M Zeigler, R Bargal, et al.
Journal of Craniofacial Genetics and Developmental Biology|January 1, 1989
Newly recognized ectrodactyly/deafness syndromeA Raas-Rothschild, A Aviram, T Ben-Ami, et al.
Pageof 4

Showing results (11-20 of 36) with videos related to

Sort By:
Pageof 4
American Journal of Medical Genetics|November 14, 2000
Contribution of connexin 26 mutations to nonsyndromic deafness in Ashkenazi patients and the variable phenotypic effect of the mutation 167delTI Lerer, M Sagi, E Malamud, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|January 16, 2003
Prenatal ultrasonographic diagnosis of atypical Nonne-Milroy lymphedemaA Lev-Sagie, Y Hamani, A Raas-Rothschild, et al.
American Journal of Medical Genetics|May 26, 1999
Agenesis of tibia with ectrodactyly/Gollop-Wolfgang complex associated with congenital heart malformations and additional skeletal abnormalitiesA Raas-Rothschild, A Nir, Z Ergaz, et al.
American Journal of Human Genetics|June 1, 1993
Negative expansion of the myotonic dystrophy unstable sequenceD Abeliovich, I Lerer, I Pashut-Lavon, et al.
Journal of Medical Genetics|December 1, 1996
Refined mapping of a gene for split hand-split foot malformation (SHFM3) on chromosome 10q25A Raas-Rothschild, S Manouvrier, M Gonzales, et al.
British Journal of Nursing (Mark Allen Publishing)|June 20, 2008
Home-based infusion therapy for patients with Fabry diseaseA Cousins, P Lee, D Rorman, et al.
The Pediatric Infectious Disease Journal|November 1, 1992
Oral ciprofloxacin in the management of chronic suppurative otitis media without cholesteatoma in children: preliminary experience in 21 childrenR Lang, S Goshen, A Raas-Rothschild, et al.
Prenatal Diagnosis|August 22, 2000
Ultrasonographic prenatal diagnosis of microcephalic osteodysplastic primordial dwarfism types I/IIIM Nadjari, S J Fasouliotis, I Ariel, et al.
Prenatal Diagnosis|March 11, 2003
Mucolipidosis III type C: first-trimester biochemical and molecular prenatal diagnosisT C Falik-Zaccai, M Zeigler, R Bargal, et al.
Journal of Craniofacial Genetics and Developmental Biology|January 1, 1989
Newly recognized ectrodactyly/deafness syndromeA Raas-Rothschild, A Aviram, T Ben-Ami, et al.
Pageof 4