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Antonio Richieri-Costa

Showing results (1-10 of 86) with videos related to

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Pro-Fono : Revista De Atualizacao Cientifica|January 15, 2009
[Aging and human communication]Antonio Richieri-Costa
American Journal of Medical Genetics. Part A|June 9, 2005
Atypical interhemispheric fusion with a cebocephalic-like functional single nostril nose and a novel SHH mutationLucilene Arilho Ribeiro, Antonio Richieri-Costa
American Journal of Medical Genetics. Part A|June 9, 2005
Cerebro-oculo-nasal syndrome, a disorder with some manifestations suggestive of the holoprosencephalic spectrum: new case and imaging review of previous casesAntonio Richieri-Costa, Lucilene Arilho Ribeiro
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|January 28, 2010
Holoprosencephaly and holoprosencephaly-like phenotypes: Review of facial and molecular findings in patients from a craniofacial hospital in BrazilAntonio Richieri-Costa, Lucilene Arilho Ribeiro
Brain & Development|September 11, 2007
Variable phenotypic manifestations of a K44N mutation in the TGIF geneAntonio Richieri-Costa, Lucilene Arilho Ribeiro
American Journal of Medical Genetics. Part A|May 31, 2008
Reply to Hunter's letter on the "misuse of the descriptor "Marfanoid""Célia M Giacheti, Antonio Richieri-Costa
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|July 21, 2006
Macrostomia, preauricular tags, and external ophthalmoplegia: a new autosomal dominant syndrome within the oculoauriculovertebral spectrum?Antonio Richieri-Costa, Lucilene Arilho Ribeiro
American Journal of Medical Genetics. Part A|June 9, 2005
Single median maxillary central incisor, hypophyseal tumor, and SHH mutationLucilene Arilho Ribeiro, Antonio Richieri-Costa
American Journal of Medical Genetics. Part A|April 15, 2009
Frontonasal dysplasia, severe neuropsychological delay, and midline central nervous system anomalies: report of 10 Brazilian male patientsMaria Leine Guion-Almeida, Antonio Richieri-Costa
International Journal of Medical Sciences|May 25, 2005
The Syndrome of Frontonasal Dysplasia, Callosal Agenesis, Basal Encephalocele, and Eye Anomalies - Phenotypic and Aetiological ConsiderationsAntonio Richieri-Costa, Maria Leine Guion-Almeida
Pageof 9

Showing results (1-10 of 86) with videos related to

Sort By:
Pageof 9
Pro-Fono : Revista De Atualizacao Cientifica|January 15, 2009
[Aging and human communication]Antonio Richieri-Costa
American Journal of Medical Genetics. Part A|June 9, 2005
Atypical interhemispheric fusion with a cebocephalic-like functional single nostril nose and a novel SHH mutationLucilene Arilho Ribeiro, Antonio Richieri-Costa
American Journal of Medical Genetics. Part A|June 9, 2005
Cerebro-oculo-nasal syndrome, a disorder with some manifestations suggestive of the holoprosencephalic spectrum: new case and imaging review of previous casesAntonio Richieri-Costa, Lucilene Arilho Ribeiro
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|January 28, 2010
Holoprosencephaly and holoprosencephaly-like phenotypes: Review of facial and molecular findings in patients from a craniofacial hospital in BrazilAntonio Richieri-Costa, Lucilene Arilho Ribeiro
Brain & Development|September 11, 2007
Variable phenotypic manifestations of a K44N mutation in the TGIF geneAntonio Richieri-Costa, Lucilene Arilho Ribeiro
American Journal of Medical Genetics. Part A|May 31, 2008
Reply to Hunter's letter on the "misuse of the descriptor "Marfanoid""Célia M Giacheti, Antonio Richieri-Costa
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|July 21, 2006
Macrostomia, preauricular tags, and external ophthalmoplegia: a new autosomal dominant syndrome within the oculoauriculovertebral spectrum?Antonio Richieri-Costa, Lucilene Arilho Ribeiro
American Journal of Medical Genetics. Part A|June 9, 2005
Single median maxillary central incisor, hypophyseal tumor, and SHH mutationLucilene Arilho Ribeiro, Antonio Richieri-Costa
American Journal of Medical Genetics. Part A|April 15, 2009
Frontonasal dysplasia, severe neuropsychological delay, and midline central nervous system anomalies: report of 10 Brazilian male patientsMaria Leine Guion-Almeida, Antonio Richieri-Costa
International Journal of Medical Sciences|May 25, 2005
The Syndrome of Frontonasal Dysplasia, Callosal Agenesis, Basal Encephalocele, and Eye Anomalies - Phenotypic and Aetiological ConsiderationsAntonio Richieri-Costa, Maria Leine Guion-Almeida
Pageof 9