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

J B Moeschler

Showing results (11-20 of 31) with videos related to

Pageof 4
Sort By:
American Journal of Diseases of Children (1960)|October 1, 1990
Reactions of mothers and medical professionals to a film about Down syndromeW C Cooley, E S Graham, J B Moeschler, et al.
Pediatrics|July 1, 1988
Rett syndrome: natural history and managementJ B Moeschler, C E Charman, S Z Berg, et al.
Annales De Genetique|January 1, 1993
A case of de novo translocation 7; 10 and the duplication 7p, deletion 10p phenotypeJ P Park, M K McDermet, J B Moeschler, et al.
Prenatal Diagnosis|September 1, 1991
Prenatal diagnosis and confirmation of trisomy 12 mosaicismJ P Park, M K McDermet, J B Moeschler, et al.
Journal of Medical Genetics|April 1, 1991
Schizophrenia and mental retardation in an adult male with a de novo interstitial deletion 9(q32q34.1)J P Park, J B Moeschler, S Z Berg, et al.
American Journal of Medical Genetics|April 29, 1998
Smith-Magenis syndrome resulting from a de novo direct insertion of proximal 17q into 17p11.2J P Park, J B Moeschler, W S Davies, et al.
Prenatal Diagnosis|July 1, 1989
Trisomy 20 mosaicism confirmed in a phenotypically normal livebornJ P Park, J B Moeschler, E Rawnsley, et al.
Clinical Genetics|January 1, 1992
A unique de novo interstitial deletion del(17)(q21.3q23) in a phenotypically abnormal infantJ P Park, J B Moeschler, S Z Berg, et al.
Clinical Genetics|February 1, 1991
Trisomy 18 and 18p- features in a case of isochromosome 18q [46,XY,i(18q)]: prenatal diagnosis and autopsy reportD H Wurster-Hill, J M Marin-Padilla, J B Moeschler, et al.
Neurology|September 30, 2011
Evidence report: Genetic and metabolic testing on children with global developmental delay [RETIRED]: report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology SocietyD J Michelson, M I Shevell, E H Sherr, et al.
Pageof 4

Showing results (11-20 of 31) with videos related to

Sort By:
Pageof 4
American Journal of Diseases of Children (1960)|October 1, 1990
Reactions of mothers and medical professionals to a film about Down syndromeW C Cooley, E S Graham, J B Moeschler, et al.
Pediatrics|July 1, 1988
Rett syndrome: natural history and managementJ B Moeschler, C E Charman, S Z Berg, et al.
Annales De Genetique|January 1, 1993
A case of de novo translocation 7; 10 and the duplication 7p, deletion 10p phenotypeJ P Park, M K McDermet, J B Moeschler, et al.
Prenatal Diagnosis|September 1, 1991
Prenatal diagnosis and confirmation of trisomy 12 mosaicismJ P Park, M K McDermet, J B Moeschler, et al.
Journal of Medical Genetics|April 1, 1991
Schizophrenia and mental retardation in an adult male with a de novo interstitial deletion 9(q32q34.1)J P Park, J B Moeschler, S Z Berg, et al.
American Journal of Medical Genetics|April 29, 1998
Smith-Magenis syndrome resulting from a de novo direct insertion of proximal 17q into 17p11.2J P Park, J B Moeschler, W S Davies, et al.
Prenatal Diagnosis|July 1, 1989
Trisomy 20 mosaicism confirmed in a phenotypically normal livebornJ P Park, J B Moeschler, E Rawnsley, et al.
Clinical Genetics|January 1, 1992
A unique de novo interstitial deletion del(17)(q21.3q23) in a phenotypically abnormal infantJ P Park, J B Moeschler, S Z Berg, et al.
Clinical Genetics|February 1, 1991
Trisomy 18 and 18p- features in a case of isochromosome 18q [46,XY,i(18q)]: prenatal diagnosis and autopsy reportD H Wurster-Hill, J M Marin-Padilla, J B Moeschler, et al.
Neurology|September 30, 2011
Evidence report: Genetic and metabolic testing on children with global developmental delay [RETIRED]: report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology SocietyD J Michelson, M I Shevell, E H Sherr, et al.
Pageof 4