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 Curtis Rogers

Showing results (1-10 of 61) with videos related to

Pageof 7
Sort By:
Case Reports in Genetics|October 24, 2012
Vici syndrome: a rare autosomal recessive syndrome with brain anomalies, cardiomyopathy, and severe intellectual disabilityR Curtis Rogers, Bridgette Aufmuth, Stephanie Monesson
Clinical Pediatrics|May 17, 2006
Congenital livedo reticularis and recurrent strokes in two unrelated young childrenGretchen Mathias, Ron Cowley, Augusto Morales, et al.
American Journal of Medical Genetics. Part A|October 30, 2013
Malformations among the X-linked intellectual disability syndromesRoger E Stevenson, Charles E Schwartz, R Curtis Rogers
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|March 3, 2015
Reply: To PMID 25266838Muralidhar Ramappa, M Edward Wilson, Rupal H Trivedi, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|October 1, 2014
Brittle cornea syndrome: a case report and comparison with Ehlers Danlos syndromeMuralidhar Ramappa, M Edward Wilson, R Curtis Rogers, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|October 29, 2010
Behavioral features in young adults with FG syndrome (Opitz-Kaveggia syndrome)John M Graham, Robin D Clark, John B Moeschler, et al.
European Journal of Medical Genetics|March 2, 2012
Seizures and X-linked intellectual disabilityRoger E Stevenson, Kenton R Holden, R Curtis Rogers, et al.
American Journal of Medical Genetics. Part A|August 13, 2005
A novel in-frame deletion in ARX is associated with lissencephaly with absent corpus callosum and hypoplastic genitaliaShambhu S Bhat, R Curtis Rogers, Kenton R Holden, et al.
American Journal of Medical Genetics. Part A|August 22, 2015
Letter to the editor regarding Disciglio et al.: interstitial 22q13 deletions not involving SHANK3 gene: a new contiguous gene syndromeKaty Phelan, Luigi Boccuto, R Curtis Rogers, et al.
Prenatal Diagnosis|July 5, 2001
Prenatal diagnosis of mosaicism for triploidy and trisomy 13M C Phelan, R Curtis Rogers, R C Michaelis, et al.
Pageof 7

Showing results (1-10 of 61) with videos related to

Sort By:
Pageof 7
Case Reports in Genetics|October 24, 2012
Vici syndrome: a rare autosomal recessive syndrome with brain anomalies, cardiomyopathy, and severe intellectual disabilityR Curtis Rogers, Bridgette Aufmuth, Stephanie Monesson
Clinical Pediatrics|May 17, 2006
Congenital livedo reticularis and recurrent strokes in two unrelated young childrenGretchen Mathias, Ron Cowley, Augusto Morales, et al.
American Journal of Medical Genetics. Part A|October 30, 2013
Malformations among the X-linked intellectual disability syndromesRoger E Stevenson, Charles E Schwartz, R Curtis Rogers
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|March 3, 2015
Reply: To PMID 25266838Muralidhar Ramappa, M Edward Wilson, Rupal H Trivedi, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|October 1, 2014
Brittle cornea syndrome: a case report and comparison with Ehlers Danlos syndromeMuralidhar Ramappa, M Edward Wilson, R Curtis Rogers, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|October 29, 2010
Behavioral features in young adults with FG syndrome (Opitz-Kaveggia syndrome)John M Graham, Robin D Clark, John B Moeschler, et al.
European Journal of Medical Genetics|March 2, 2012
Seizures and X-linked intellectual disabilityRoger E Stevenson, Kenton R Holden, R Curtis Rogers, et al.
American Journal of Medical Genetics. Part A|August 13, 2005
A novel in-frame deletion in ARX is associated with lissencephaly with absent corpus callosum and hypoplastic genitaliaShambhu S Bhat, R Curtis Rogers, Kenton R Holden, et al.
American Journal of Medical Genetics. Part A|August 22, 2015
Letter to the editor regarding Disciglio et al.: interstitial 22q13 deletions not involving SHANK3 gene: a new contiguous gene syndromeKaty Phelan, Luigi Boccuto, R Curtis Rogers, et al.
Prenatal Diagnosis|July 5, 2001
Prenatal diagnosis of mosaicism for triploidy and trisomy 13M C Phelan, R Curtis Rogers, R C Michaelis, et al.
Pageof 7