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

Maria Rita Passos-Bueno

Showing results (1-10 of 156) with videos related to

Pageof 16
Sort By:
Genetics and Molecular Biology|August 31, 2016
Neuromuscular disorders: genes, genetic counseling and therapeutic trialsMayana Zatz, Maria Rita Passos-Bueno, Mariz Vainzof
Discover Mental Health|October 20, 2023
Dystrophin genetic variants and autismMaria Rita Passos-Bueno, Claudia Ismania Samogy Costa, Mayana Zatz
American Journal of Medical Genetics. Part A|July 18, 2009
Syndromes of the first and second pharyngeal arches: A reviewMaria Rita Passos-Bueno, Camila C Ornelas, Roberto D Fanganiello
European Journal of Human Genetics : EJHG|September 16, 2004
A new form of autosomal dominant limb-girdle muscular dystrophy (LGMD1G) with progressive fingers and toes flexion limitation maps to chromosome 4p21Alessandra Starling, Fernando Kok, Maria Rita Passos-Bueno, et al.
European Journal of Human Genetics : EJHG|August 27, 2003
Parental origin of mutations in sporadic cases of Treacher Collins syndromeAlessandra Splendore, Ethylin Wang Jabs, Têmis Maria Félix, et al.
American Journal of Medical Genetics. Part A|February 18, 2017
The recurrent PPP1CB mutation p.Pro49Arg in an additional Noonan-like syndrome individual: Broadening the clinical phenotypeDébora Bertola, Guilherme Yamamoto, Michelle Buscarilli, et al.
Frontiers of Oral Biology|April 9, 2008
Genetics of craniosynostosis: genes, syndromes, mutations and genotype-phenotype correlationsMaria Rita Passos-Bueno, Andréa L Sertié, Fernanda S Jehee, et al.
BMC Research Notes|September 23, 2010
Collybistin and gephyrin are novel components of the eukaryotic translation initiation factor 3 complexAndrea L Sertie, Gustavo de Alencastro, Vanessa J De Paula, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|September 7, 2006
Further evidence of association between mutations in FGFR2 and syndromic craniosynostosis with sacrococcygeal eversionNélio A J Oliveira, Luís G Alonso, Roberto D Fanganiello, et al.
Autism Research : Official Journal of the International Society for Autism Research|June 27, 2013
Stem cells as a good tool to investigate dysregulated biological systems in autism spectrum disordersKarina Griesi-Oliveira, Daniele Yumi Sunaga, Lucas Alvizi, et al.
Pageof 16

Showing results (1-10 of 156) with videos related to

Sort By:
Pageof 16
Genetics and Molecular Biology|August 31, 2016
Neuromuscular disorders: genes, genetic counseling and therapeutic trialsMayana Zatz, Maria Rita Passos-Bueno, Mariz Vainzof
Discover Mental Health|October 20, 2023
Dystrophin genetic variants and autismMaria Rita Passos-Bueno, Claudia Ismania Samogy Costa, Mayana Zatz
American Journal of Medical Genetics. Part A|July 18, 2009
Syndromes of the first and second pharyngeal arches: A reviewMaria Rita Passos-Bueno, Camila C Ornelas, Roberto D Fanganiello
European Journal of Human Genetics : EJHG|September 16, 2004
A new form of autosomal dominant limb-girdle muscular dystrophy (LGMD1G) with progressive fingers and toes flexion limitation maps to chromosome 4p21Alessandra Starling, Fernando Kok, Maria Rita Passos-Bueno, et al.
European Journal of Human Genetics : EJHG|August 27, 2003
Parental origin of mutations in sporadic cases of Treacher Collins syndromeAlessandra Splendore, Ethylin Wang Jabs, Têmis Maria Félix, et al.
American Journal of Medical Genetics. Part A|February 18, 2017
The recurrent PPP1CB mutation p.Pro49Arg in an additional Noonan-like syndrome individual: Broadening the clinical phenotypeDébora Bertola, Guilherme Yamamoto, Michelle Buscarilli, et al.
Frontiers of Oral Biology|April 9, 2008
Genetics of craniosynostosis: genes, syndromes, mutations and genotype-phenotype correlationsMaria Rita Passos-Bueno, Andréa L Sertié, Fernanda S Jehee, et al.
BMC Research Notes|September 23, 2010
Collybistin and gephyrin are novel components of the eukaryotic translation initiation factor 3 complexAndrea L Sertie, Gustavo de Alencastro, Vanessa J De Paula, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|September 7, 2006
Further evidence of association between mutations in FGFR2 and syndromic craniosynostosis with sacrococcygeal eversionNélio A J Oliveira, Luís G Alonso, Roberto D Fanganiello, et al.
Autism Research : Official Journal of the International Society for Autism Research|June 27, 2013
Stem cells as a good tool to investigate dysregulated biological systems in autism spectrum disordersKarina Griesi-Oliveira, Daniele Yumi Sunaga, Lucas Alvizi, et al.
Pageof 16