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

B Gener

Showing results (1-10 of 11) with videos related to

Pageof 2
Sort By:
The Journal of Infection|March 1, 1997
Bacterial sinusitis associated with subacute, granulomatous thyroiditisJ Collazos, B Gener, J de Miguel
Revista De Neurologia|September 20, 2001
[Can acute disseminated encephalomyelitis progress in a deferred way?]B Gener, C Garaizar-Axpe, C Ruiz Espinosa, et al.
Pediatric Neurology|March 29, 2001
Multilocular hydrocephalus: ultrasound studies of origin and developmentJ M Prats, J López-Heredia, B Gener, et al.
Revista De Neurologia|February 1, 2000
[Neuropediatric clinical practice in a tertiary hospital of Basque Country]C Garaizar, M J Martínez-González, I Sobradillo, et al.
Revue D'Epidemiologie Et De Sante Publique|February 14, 2006
Trends and geographic inequalities in the prevalence of Down syndrome in Europe, 1980-1999H Dolk, M Loane, E Garne, et al.
Clinical Genetics|March 4, 2016
The MECP2 variant c.925C>T (p.Arg309Trp) causes intellectual disability in both males and females without classic features of Rett syndromeB Schönewolf-Greulich, M-I Tejada, K Stephens, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|December 25, 2004
Prenatal diagnosis of severe structural congenital malformations in EuropeE Garne, M Loane, H Dolk, et al.
Mutation Research. Genetic Toxicology and Environmental Mutagenesis|April 9, 2020
The Iberian legacy into a young genetic xeroderma pigmentosum cluster in central BrazilL P Castro, M Sahbatou, F S G Kehdy, et al.
European Journal of Medical Genetics|April 24, 2012
Xq28 duplications including MECP2 in five females: Expanding the phenotype to severe mental retardationE K Bijlsma, A Collins, F T Papa, et al.
Human Mutation|November 7, 2009
Mutation update for the CSB/ERCC6 and CSA/ERCC8 genes involved in Cockayne syndromeV Laugel, C Dalloz, M Durand, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
The Journal of Infection|March 1, 1997
Bacterial sinusitis associated with subacute, granulomatous thyroiditisJ Collazos, B Gener, J de Miguel
Revista De Neurologia|September 20, 2001
[Can acute disseminated encephalomyelitis progress in a deferred way?]B Gener, C Garaizar-Axpe, C Ruiz Espinosa, et al.
Pediatric Neurology|March 29, 2001
Multilocular hydrocephalus: ultrasound studies of origin and developmentJ M Prats, J López-Heredia, B Gener, et al.
Revista De Neurologia|February 1, 2000
[Neuropediatric clinical practice in a tertiary hospital of Basque Country]C Garaizar, M J Martínez-González, I Sobradillo, et al.
Revue D'Epidemiologie Et De Sante Publique|February 14, 2006
Trends and geographic inequalities in the prevalence of Down syndrome in Europe, 1980-1999H Dolk, M Loane, E Garne, et al.
Clinical Genetics|March 4, 2016
The MECP2 variant c.925C>T (p.Arg309Trp) causes intellectual disability in both males and females without classic features of Rett syndromeB Schönewolf-Greulich, M-I Tejada, K Stephens, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|December 25, 2004
Prenatal diagnosis of severe structural congenital malformations in EuropeE Garne, M Loane, H Dolk, et al.
Mutation Research. Genetic Toxicology and Environmental Mutagenesis|April 9, 2020
The Iberian legacy into a young genetic xeroderma pigmentosum cluster in central BrazilL P Castro, M Sahbatou, F S G Kehdy, et al.
European Journal of Medical Genetics|April 24, 2012
Xq28 duplications including MECP2 in five females: Expanding the phenotype to severe mental retardationE K Bijlsma, A Collins, F T Papa, et al.
Human Mutation|November 7, 2009
Mutation update for the CSB/ERCC6 and CSA/ERCC8 genes involved in Cockayne syndromeV Laugel, C Dalloz, M Durand, et al.
Pageof 2