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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 mutation
Lucilene 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 cases
Antonio 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 Brazil
Antonio Richieri-Costa, Lucilene Arilho Ribeiro
Brain & Development
|
September 11, 2007
Variable phenotypic manifestations of a K44N mutation in the TGIF gene
Antonio 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 mutation
Lucilene 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 patients
Maria 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 Considerations
Antonio Richieri-Costa, Maria Leine Guion-Almeida
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of 9
Search research articles
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Showing results (1-10 of 86) with videos related to
Sort By:
Page
of 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 mutation
Lucilene 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 cases
Antonio 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 Brazil
Antonio Richieri-Costa, Lucilene Arilho Ribeiro
Brain & Development
|
September 11, 2007
Variable phenotypic manifestations of a K44N mutation in the TGIF gene
Antonio 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 mutation
Lucilene 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 patients
Maria 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 Considerations
Antonio Richieri-Costa, Maria Leine Guion-Almeida
Page
of 9