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

W B Dobyns

Showing results (31-40 of 151) with videos related to

Pageof 16
Sort By:
Neurology|July 23, 2003
Polyalanine expansion of ARX associated with cryptogenic West syndromeM Kato, S Das, K Petras, et al.
Human Genetics|August 1, 1988
Familial pericentric and paracentric inversions of chromosome 1D D Johnson, W B Dobyns, H Gordon, et al.
American Journal of Human Genetics|August 1, 1997
Identification of a duplication of Xq28 associated with bilateral periventricular nodular heterotopiaJ M Fink, W B Dobyns, R Guerrini, et al.
American Journal of Human Genetics|January 1, 1992
Microdeletions of chromosome 17p13 as a cause of isolated lissencephalyS A Ledbetter, A Kuwano, W B Dobyns, et al.
Neurology|August 15, 2001
LIS1 missense mutations cause milder lissencephaly phenotypes including a child with normal IQR J Leventer, C Cardoso, D H Ledbetter, et al.
Journal of Medical Genetics|May 10, 2005
Oculocerebrocutaneous syndrome: the brain malformation defines a core phenotypeU Moog, M C Jones, L M Bird, et al.
Journal of Child Neurology|August 2, 2000
Diffuse polymicrogyria associated with congenital hydrocephalus, craniosynostosis, severe mental retardation, and minor facial and genital anomaliesL Pavone, R Rizzo, P Pavone, et al.
Neuroradiology|October 1, 1996
Congenital pontocerebellar atrophy in three patients: clinical, radiologic and etiologic considerationsN Zelnik, W B Dobyns, S L Forem, et al.
Journal of Child Neurology|January 1, 1990
Isolated lissencephaly: report of four patients from two unrelated familiesL Pavone, F Gullotta, G Incorpora, et al.
Pediatric Neurology|May 1, 1997
Valproate-induced liver failure in one of two siblings with Alpers diseaseM J Schwabe, W B Dobyns, B Burke, et al.
Pageof 16

Showing results (31-40 of 151) with videos related to

Sort By:
Pageof 16
Neurology|July 23, 2003
Polyalanine expansion of ARX associated with cryptogenic West syndromeM Kato, S Das, K Petras, et al.
Human Genetics|August 1, 1988
Familial pericentric and paracentric inversions of chromosome 1D D Johnson, W B Dobyns, H Gordon, et al.
American Journal of Human Genetics|August 1, 1997
Identification of a duplication of Xq28 associated with bilateral periventricular nodular heterotopiaJ M Fink, W B Dobyns, R Guerrini, et al.
American Journal of Human Genetics|January 1, 1992
Microdeletions of chromosome 17p13 as a cause of isolated lissencephalyS A Ledbetter, A Kuwano, W B Dobyns, et al.
Neurology|August 15, 2001
LIS1 missense mutations cause milder lissencephaly phenotypes including a child with normal IQR J Leventer, C Cardoso, D H Ledbetter, et al.
Journal of Medical Genetics|May 10, 2005
Oculocerebrocutaneous syndrome: the brain malformation defines a core phenotypeU Moog, M C Jones, L M Bird, et al.
Journal of Child Neurology|August 2, 2000
Diffuse polymicrogyria associated with congenital hydrocephalus, craniosynostosis, severe mental retardation, and minor facial and genital anomaliesL Pavone, R Rizzo, P Pavone, et al.
Neuroradiology|October 1, 1996
Congenital pontocerebellar atrophy in three patients: clinical, radiologic and etiologic considerationsN Zelnik, W B Dobyns, S L Forem, et al.
Journal of Child Neurology|January 1, 1990
Isolated lissencephaly: report of four patients from two unrelated familiesL Pavone, F Gullotta, G Incorpora, et al.
Pediatric Neurology|May 1, 1997
Valproate-induced liver failure in one of two siblings with Alpers diseaseM J Schwabe, W B Dobyns, B Burke, et al.
Pageof 16