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 M Gardner

Showing results (1-10 of 9) with videos related to

Pageof 1
Sort By:
American Journal of Medical Genetics. Part A|March 26, 2003
Another explanation for familial Cornelia de Lange syndromeR J M Gardner
Journal of Medical Genetics|March 4, 2008
"SCA16" is really SCA15R J M Gardner
Fetal Diagnosis and Therapy|July 29, 2010
Trisomy 16 mosaicism at chorionic villus sampling and amniocentesis with a normal physical and intellectual outcomeD Coman, R J M Gardner, M D Pertile, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 11, 2008
A new dominantly inherited pure cerebellar ataxia, SCA 30E Storey, M Bahlo, M Fahey, et al.
Scientific Reports|January 7, 2017
A novel role for the DNA repair gene Rad51 in Netrin-1 signallingK A Glendining, D Markie, R J M Gardner, et al.
Internal Medicine Journal|December 6, 2003
Novel p53 germline mutation in a patient with Li-Fraumeni syndromeS S Wong, G Lozano, C L Gaff, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 18, 2005
Superior verbal ability and nonverbal learning disability in a child with a novel 17p12p13.1 deletionD L Steele, A K Chisholm, J D R McGhie, et al.
Journal of Medical Genetics|August 3, 2005
Familial scaphocephaly syndrome caused by a novel mutation in the FGFR2 tyrosine kinase domainG McGillivray, R Savarirayan, T C Cox, et al.
Journal of Medical Genetics|November 19, 2008
Detection of cryptic pathogenic copy number variations and constitutional loss of heterozygosity using high resolution SNP microarray analysis in 117 patients referred for cytogenetic analysis and impact on clinical practiceD L Bruno, D Ganesamoorthy, J Schoumans, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
American Journal of Medical Genetics. Part A|March 26, 2003
Another explanation for familial Cornelia de Lange syndromeR J M Gardner
Journal of Medical Genetics|March 4, 2008
"SCA16" is really SCA15R J M Gardner
Fetal Diagnosis and Therapy|July 29, 2010
Trisomy 16 mosaicism at chorionic villus sampling and amniocentesis with a normal physical and intellectual outcomeD Coman, R J M Gardner, M D Pertile, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 11, 2008
A new dominantly inherited pure cerebellar ataxia, SCA 30E Storey, M Bahlo, M Fahey, et al.
Scientific Reports|January 7, 2017
A novel role for the DNA repair gene Rad51 in Netrin-1 signallingK A Glendining, D Markie, R J M Gardner, et al.
Internal Medicine Journal|December 6, 2003
Novel p53 germline mutation in a patient with Li-Fraumeni syndromeS S Wong, G Lozano, C L Gaff, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 18, 2005
Superior verbal ability and nonverbal learning disability in a child with a novel 17p12p13.1 deletionD L Steele, A K Chisholm, J D R McGhie, et al.
Journal of Medical Genetics|August 3, 2005
Familial scaphocephaly syndrome caused by a novel mutation in the FGFR2 tyrosine kinase domainG McGillivray, R Savarirayan, T C Cox, et al.
Journal of Medical Genetics|November 19, 2008
Detection of cryptic pathogenic copy number variations and constitutional loss of heterozygosity using high resolution SNP microarray analysis in 117 patients referred for cytogenetic analysis and impact on clinical practiceD L Bruno, D Ganesamoorthy, J Schoumans, et al.
Pageof 1