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

M Zappella

Showing results (41-50 of 48) with videos related to

Pageof 5
Sort By:
You have reached the last page of results.This site can display upto 48 results.
Journal of Medical Genetics|February 4, 2005
CDKL5/STK9 is mutated in Rett syndrome variant with infantile spasmsE Scala, F Ariani, F Mari, et al.
Orphanet Journal of Rare Diseases|September 30, 2016
Rett syndrome: a wide clinical and autonomic pictureG Pini, S Bigoni, L Congiu, et al.
Clinical Genetics|February 5, 2005
Germline mosaicism in Rett syndrome identified by prenatal diagnosisF Mari, R Caselli, S Russo, et al.
Human Molecular Genetics|April 10, 1999
Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair StudyA Philippe, M Martinez, M Guilloud-Bataille, et al.
Journal of Molecular Medicine (Berlin, Germany)|March 28, 2001
Mutation analysis of the MECP2 gene in British and Italian Rett syndrome femalesM Vacca, F Filippini, A Budillon, et al.
American Journal of Medical Genetics. Part A|December 21, 2002
18q-syndrome and ectodermal dysplasia syndrome: description of a child and his familyR Zannolli, M Pierluigi, L Pucci, et al.
Journal of Medical Genetics|November 25, 2003
Hereditary xanthinuria type II associated with mental delay, autism, cortical renal cysts, nephrocalcinosis, osteopenia, and hair and teeth defectsR Zannolli, V Micheli, M A Mazzei, et al.
Brain & Development|December 12, 2001
MECP2 gene mutation analysis in the British and Italian Rett Syndrome patients: hot spot map of the most recurrent mutations and bioinformatic analysis of a new MECP2 conserved regionM Vacca, F Filippini, A Budillon, et al.
Pageof 5

Showing results (41-50 of 48) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 48 results.
Journal of Medical Genetics|February 4, 2005
CDKL5/STK9 is mutated in Rett syndrome variant with infantile spasmsE Scala, F Ariani, F Mari, et al.
Orphanet Journal of Rare Diseases|September 30, 2016
Rett syndrome: a wide clinical and autonomic pictureG Pini, S Bigoni, L Congiu, et al.
Clinical Genetics|February 5, 2005
Germline mosaicism in Rett syndrome identified by prenatal diagnosisF Mari, R Caselli, S Russo, et al.
Human Molecular Genetics|April 10, 1999
Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair StudyA Philippe, M Martinez, M Guilloud-Bataille, et al.
Journal of Molecular Medicine (Berlin, Germany)|March 28, 2001
Mutation analysis of the MECP2 gene in British and Italian Rett syndrome femalesM Vacca, F Filippini, A Budillon, et al.
American Journal of Medical Genetics. Part A|December 21, 2002
18q-syndrome and ectodermal dysplasia syndrome: description of a child and his familyR Zannolli, M Pierluigi, L Pucci, et al.
Journal of Medical Genetics|November 25, 2003
Hereditary xanthinuria type II associated with mental delay, autism, cortical renal cysts, nephrocalcinosis, osteopenia, and hair and teeth defectsR Zannolli, V Micheli, M A Mazzei, et al.
Brain & Development|December 12, 2001
MECP2 gene mutation analysis in the British and Italian Rett Syndrome patients: hot spot map of the most recurrent mutations and bioinformatic analysis of a new MECP2 conserved regionM Vacca, F Filippini, A Budillon, et al.
Pageof 5