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

P L Mills

Showing results (1-10 of 7) with videos related to

Pageof 1
Sort By:
American Journal of Medical Genetics|June 13, 1997
Urorectal septal defects in a female and her offspringP L Mills, E Pergament
FEBS Letters|May 16, 1994
Deletion analysis of the dystrophin-actin binding domainK Corrado, P L Mills, J S Chamberlain
American Journal of Medical Genetics|July 14, 2001
X-linked malformations of cortical developmentR J Leventer, P L Mills, W B Dobyns
The Journal of Cell Biology|August 1, 1996
Transgenic mdx mice expressing dystrophin with a deletion in the actin-binding domain display a "mild Becker" phenotypeK Corrado, J A Rafael, P L Mills, et al.
Neurology|July 27, 2001
Incomplete penetrance with normal MRI in a woman with germline mutation of the DCX geneL Demelas, G Serra, M Conti, et al.
European Journal of Human Genetics : EJHG|February 15, 2001
Mutation analysis of the DCX gene and genotype/phenotype correlation in subcortical band heterotopiaN Matsumoto, R J Leventer, J A Kuc, et al.
Human Molecular Genetics|December 15, 2000
The location and type of mutation predict malformation severity in isolated lissencephaly caused by abnormalities within the LIS1 geneC Cardoso, R J Leventer, N Matsumoto, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
American Journal of Medical Genetics|June 13, 1997
Urorectal septal defects in a female and her offspringP L Mills, E Pergament
FEBS Letters|May 16, 1994
Deletion analysis of the dystrophin-actin binding domainK Corrado, P L Mills, J S Chamberlain
American Journal of Medical Genetics|July 14, 2001
X-linked malformations of cortical developmentR J Leventer, P L Mills, W B Dobyns
The Journal of Cell Biology|August 1, 1996
Transgenic mdx mice expressing dystrophin with a deletion in the actin-binding domain display a "mild Becker" phenotypeK Corrado, J A Rafael, P L Mills, et al.
Neurology|July 27, 2001
Incomplete penetrance with normal MRI in a woman with germline mutation of the DCX geneL Demelas, G Serra, M Conti, et al.
European Journal of Human Genetics : EJHG|February 15, 2001
Mutation analysis of the DCX gene and genotype/phenotype correlation in subcortical band heterotopiaN Matsumoto, R J Leventer, J A Kuc, et al.
Human Molecular Genetics|December 15, 2000
The location and type of mutation predict malformation severity in isolated lissencephaly caused by abnormalities within the LIS1 geneC Cardoso, R J Leventer, N Matsumoto, et al.
Pageof 1