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 J Hagerman

Showing results (51-60 of 109) with videos related to

Pageof 11
Sort By:
American Journal of Medical Genetics|February 1, 1991
Heterozygous fragile X female: historical, physical, cognitive, and cytogenetic featuresA Cronister, R Schreiner, M Wittenberger, et al.
American Journal of Medical Genetics|July 15, 1994
Emotional and neurocognitive deficits in fragile XW E Sobesky, B F Pennington, D Porter, et al.
Pediatrics|March 1, 1992
Girls with fragile X syndrome: physical and neurocognitive status and outcomeR J Hagerman, C Jackson, K Amiri, et al.
Neuroepidemiology|February 24, 2006
Prevalence of FMR1 repeat expansions in movement disorders. A systematic reviewD A Hall, R J Hagerman, P J Hagerman, et al.
Cognitive Neuropsychology|October 15, 2010
Discourse processing in women with fragile x syndrome: evidence for a deficit establishing coherenceJ A Simon, J M Keenan, B F Pennington, et al.
American Journal of Medical Genetics. Part A|March 26, 2003
Relationship of deficits of FMR1 gene specific protein with physical phenotype of fragile X males and females in pedigrees: a new perspectiveD Z Loesch, R M Huggins, Q M Bui, et al.
Journal of Intellectual Disability Research : JIDR|October 10, 2015
Characterising repetitive behaviours in young boys with fragile X syndromeA Oakes, A J Thurman, A McDuffie, et al.
Clinical Genetics|January 17, 2013
Fragile X syndrome: clinical, cytogenetic and molecular screening among autism spectrum disorder children in IndonesiaT I Winarni, A Utari, F E P Mundhofir, et al.
American Journal of Medical Genetics|August 1, 1989
Longitudinal IQ changes in fragile X malesR J Hagerman, R A Schreiner, M B Kemper, et al.
Clinical Genetics|June 22, 2013
A family with two female siblings with compound heterozygous FMR1 premutation allelesK Basuta, R Lozano, A Schneider, et al.
Pageof 11

Showing results (51-60 of 109) with videos related to

Sort By:
Pageof 11
American Journal of Medical Genetics|February 1, 1991
Heterozygous fragile X female: historical, physical, cognitive, and cytogenetic featuresA Cronister, R Schreiner, M Wittenberger, et al.
American Journal of Medical Genetics|July 15, 1994
Emotional and neurocognitive deficits in fragile XW E Sobesky, B F Pennington, D Porter, et al.
Pediatrics|March 1, 1992
Girls with fragile X syndrome: physical and neurocognitive status and outcomeR J Hagerman, C Jackson, K Amiri, et al.
Neuroepidemiology|February 24, 2006
Prevalence of FMR1 repeat expansions in movement disorders. A systematic reviewD A Hall, R J Hagerman, P J Hagerman, et al.
Cognitive Neuropsychology|October 15, 2010
Discourse processing in women with fragile x syndrome: evidence for a deficit establishing coherenceJ A Simon, J M Keenan, B F Pennington, et al.
American Journal of Medical Genetics. Part A|March 26, 2003
Relationship of deficits of FMR1 gene specific protein with physical phenotype of fragile X males and females in pedigrees: a new perspectiveD Z Loesch, R M Huggins, Q M Bui, et al.
Journal of Intellectual Disability Research : JIDR|October 10, 2015
Characterising repetitive behaviours in young boys with fragile X syndromeA Oakes, A J Thurman, A McDuffie, et al.
Clinical Genetics|January 17, 2013
Fragile X syndrome: clinical, cytogenetic and molecular screening among autism spectrum disorder children in IndonesiaT I Winarni, A Utari, F E P Mundhofir, et al.
American Journal of Medical Genetics|August 1, 1989
Longitudinal IQ changes in fragile X malesR J Hagerman, R A Schreiner, M B Kemper, et al.
Clinical Genetics|June 22, 2013
A family with two female siblings with compound heterozygous FMR1 premutation allelesK Basuta, R Lozano, A Schneider, et al.
Pageof 11