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Artigo de periodico
Severe midline craniofacial anomalies: overlap with Pai syndrome (2009)
Guion-Almeida, Maria Leine; Richieri-Costa, Antonio
Source: Clinical Dysmorphology. Unidade: HRAC
Subjects: ANORMALIDADES CRANIOFACIAIS, FACE (ANORMALIDADES), CRÂNIO (ANORMALIDADES)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUION-ALMEIDA, Maria Leine e RICHIERI-COSTA, Antonio. Severe midline craniofacial anomalies: overlap with Pai syndrome. Clinical Dysmorphology, v. 18, n. 3, p. 154-157, 2009Tradução . . Disponível em: https://doi.org/10.1097/MCD.0b013e32832443c8. Acesso em: 04 out. 2024.
APA
Guion-Almeida, M. L., & Richieri-Costa, A. (2009). Severe midline craniofacial anomalies: overlap with Pai syndrome. Clinical Dysmorphology, 18( 3), 154-157. doi:10.1097/MCD.0b013e32832443c8
NLM
Guion-Almeida ML, Richieri-Costa A. Severe midline craniofacial anomalies: overlap with Pai syndrome [Internet]. Clinical Dysmorphology. 2009 ; 18( 3): 154-157.[citado 2024 out. 04 ] Available from: https://doi.org/10.1097/MCD.0b013e32832443c8
Vancouver
Guion-Almeida ML, Richieri-Costa A. Severe midline craniofacial anomalies: overlap with Pai syndrome [Internet]. Clinical Dysmorphology. 2009 ; 18( 3): 154-157.[citado 2024 out. 04 ] Available from: https://doi.org/10.1097/MCD.0b013e32832443c8
Artigo de periodico
Auriculo-condylar syndrome: mapping of a first locus and evidence for genetic heterogeneity (2008)
Masotti, Cibele; Oliveira, Karina G.; Poerner, Fabiana; Splendore, Alessandra; Souza, Josiane; Freitas, Renato da Silva; Zechi-Ceide, Roseli Maria; Guion-Almeida, Maria Leine; Passos-Bueno, Maria Rita
Source: European Journal of Human Genetics. Unidades: HRAC, IB
Subjects: GENÉTICA, MAPEAMENTO CROMOSSÔMICO, DISOSTOSE MANDIBULOFACIAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MASOTTI, Cibele et al. Auriculo-condylar syndrome: mapping of a first locus and evidence for genetic heterogeneity. European Journal of Human Genetics, v. 16, n. 2, p. 145-152, 2008Tradução . . Disponível em: https://doi.org/10.1038/sj.ejhg.5201955. Acesso em: 04 out. 2024.
APA
Masotti, C., Oliveira, K. G., Poerner, F., Splendore, A., Souza, J., Freitas, R. da S., et al. (2008). Auriculo-condylar syndrome: mapping of a first locus and evidence for genetic heterogeneity. European Journal of Human Genetics, 16( 2), 145-152. doi:10.1038/sj.ejhg.5201955
NLM
Masotti C, Oliveira KG, Poerner F, Splendore A, Souza J, Freitas R da S, Zechi-Ceide RM, Guion-Almeida ML, Passos-Bueno MR. Auriculo-condylar syndrome: mapping of a first locus and evidence for genetic heterogeneity [Internet]. European Journal of Human Genetics. 2008 ; 16( 2): 145-152.[citado 2024 out. 04 ] Available from: https://doi.org/10.1038/sj.ejhg.5201955
Vancouver
Masotti C, Oliveira KG, Poerner F, Splendore A, Souza J, Freitas R da S, Zechi-Ceide RM, Guion-Almeida ML, Passos-Bueno MR. Auriculo-condylar syndrome: mapping of a first locus and evidence for genetic heterogeneity [Internet]. European Journal of Human Genetics. 2008 ; 16( 2): 145-152.[citado 2024 out. 04 ] Available from: https://doi.org/10.1038/sj.ejhg.5201955
Artigo de periodico
Holoprosencephaly spectrum, ano/microphthalmia, and first branchial arch defects: evidence for a new disorder (2008)
Guion-Almeida, Maria Leine; Richieri-Costa, Antonio; Ceide, Roseli Maria Zechi
Source: Clinical Dysmorphology. Unidade: HRAC
Subjects: HOLOPROSENCEFALIA, ANORMALIDADES CRANIOFACIAIS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUION-ALMEIDA, Maria Leine e RICHIERI-COSTA, Antonio e CEIDE, Roseli Maria Zechi. Holoprosencephaly spectrum, ano/microphthalmia, and first branchial arch defects: evidence for a new disorder. Clinical Dysmorphology, v. 17, n. Ja 2008, p. 41-46, 2008Tradução . . Disponível em: https://doi.org/10.1097/mcd.0b013e328274244f. Acesso em: 04 out. 2024.
APA
Guion-Almeida, M. L., Richieri-Costa, A., & Ceide, R. M. Z. (2008). Holoprosencephaly spectrum, ano/microphthalmia, and first branchial arch defects: evidence for a new disorder. Clinical Dysmorphology, 17( Ja 2008), 41-46. doi:10.1097/mcd.0b013e328274244f
NLM
Guion-Almeida ML, Richieri-Costa A, Ceide RMZ. Holoprosencephaly spectrum, ano/microphthalmia, and first branchial arch defects: evidence for a new disorder [Internet]. Clinical Dysmorphology. 2008 ; 17( Ja 2008): 41-46.[citado 2024 out. 04 ] Available from: https://doi.org/10.1097/mcd.0b013e328274244f
Vancouver
Guion-Almeida ML, Richieri-Costa A, Ceide RMZ. Holoprosencephaly spectrum, ano/microphthalmia, and first branchial arch defects: evidence for a new disorder [Internet]. Clinical Dysmorphology. 2008 ; 17( Ja 2008): 41-46.[citado 2024 out. 04 ] Available from: https://doi.org/10.1097/mcd.0b013e328274244f
Artigo de periodico
Oral teratoma, dextrocardia, and congenital heart defect: a nonrandom association or serendipity? (2008)
Richieri-Costa, Antonio; Ceide, Roseli Maria Zechi; Guion-Almeida, Maria Leine
Source: Clinical Dysmorphology. Unidade: HRAC
Subjects: ANORMALIDADES MÚLTIPLAS, TERATOMA, ANORMALIDADES CARDIOVASCULARES, NEOPLASIAS BUCAIS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RICHIERI-COSTA, Antonio e CEIDE, Roseli Maria Zechi e GUION-ALMEIDA, Maria Leine. Oral teratoma, dextrocardia, and congenital heart defect: a nonrandom association or serendipity?. Clinical Dysmorphology, v. 17, n. 2, p. 149-150, 2008Tradução . . Disponível em: https://doi.org/10.1097/MCD.0b013e3282f254b7. Acesso em: 04 out. 2024.
APA
Richieri-Costa, A., Ceide, R. M. Z., & Guion-Almeida, M. L. (2008). Oral teratoma, dextrocardia, and congenital heart defect: a nonrandom association or serendipity? Clinical Dysmorphology, 17( 2), 149-150. doi:10.1097/MCD.0b013e3282f254b7
NLM
Richieri-Costa A, Ceide RMZ, Guion-Almeida ML. Oral teratoma, dextrocardia, and congenital heart defect: a nonrandom association or serendipity? [Internet]. Clinical Dysmorphology. 2008 ; 17( 2): 149-150.[citado 2024 out. 04 ] Available from: https://doi.org/10.1097/MCD.0b013e3282f254b7
Vancouver
Richieri-Costa A, Ceide RMZ, Guion-Almeida ML. Oral teratoma, dextrocardia, and congenital heart defect: a nonrandom association or serendipity? [Internet]. Clinical Dysmorphology. 2008 ; 17( 2): 149-150.[citado 2024 out. 04 ] Available from: https://doi.org/10.1097/MCD.0b013e3282f254b7
Artigo de periodico
Unusual phenotype in a female patient with a Gly25Ala substitution in the signal peptide region of the COL2A1 gene (2008)
Ceide, Roseli Maria Zechi; Oliveira, Nélio Alessandro de Jesus; Guion-Almeida, Maria Leine; Antunes, Luis Fernando Benedito Bergami; Richieri-Costa, Antonio; Passos-Bueno, Maria Rita
Source: Clinical Dysmorphology. Unidades: HRAC, IB
Subjects: ANORMALIDADES MÚLTIPLAS, FENÓTIPOS, GENES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CEIDE, Roseli Maria Zechi et al. Unusual phenotype in a female patient with a Gly25Ala substitution in the signal peptide region of the COL2A1 gene. Clinical Dysmorphology, v. 17, n. 3, p. 225-226, 2008Tradução . . Disponível em: https://doi.org/10.1097/mcd.0b013e3282fe1b8e. Acesso em: 04 out. 2024.
APA
Ceide, R. M. Z., Oliveira, N. A. de J., Guion-Almeida, M. L., Antunes, L. F. B. B., Richieri-Costa, A., & Passos-Bueno, M. R. (2008). Unusual phenotype in a female patient with a Gly25Ala substitution in the signal peptide region of the COL2A1 gene. Clinical Dysmorphology, 17( 3), 225-226. doi:10.1097/mcd.0b013e3282fe1b8e
NLM
Ceide RMZ, Oliveira NA de J, Guion-Almeida ML, Antunes LFBB, Richieri-Costa A, Passos-Bueno MR. Unusual phenotype in a female patient with a Gly25Ala substitution in the signal peptide region of the COL2A1 gene [Internet]. Clinical Dysmorphology. 2008 ; 17( 3): 225-226.[citado 2024 out. 04 ] Available from: https://doi.org/10.1097/mcd.0b013e3282fe1b8e
Vancouver
Ceide RMZ, Oliveira NA de J, Guion-Almeida ML, Antunes LFBB, Richieri-Costa A, Passos-Bueno MR. Unusual phenotype in a female patient with a Gly25Ala substitution in the signal peptide region of the COL2A1 gene [Internet]. Clinical Dysmorphology. 2008 ; 17( 3): 225-226.[citado 2024 out. 04 ] Available from: https://doi.org/10.1097/mcd.0b013e3282fe1b8e
Artigo de periodico
Hydrocephalus and moderate mental retardation in a boy with Van der Woude phenotype and IRF6 gene mutation (2007)
Ceide, Roseli Maria Zechi; Guion-Almeida, Maria Leine; Rodini, Elaine Sbroggio de Oliveira; Oliveira, Nélio Alessandro de Jesus; Passos-Bueno, Maria Rita
Source: Clinical Dysmorphology. Unidades: HRAC, IB
Subjects: MUTAÇÃO GENÉTICA, RETARDO MENTAL, ANORMALIDADES CRANIOFACIAIS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CEIDE, Roseli Maria Zechi et al. Hydrocephalus and moderate mental retardation in a boy with Van der Woude phenotype and IRF6 gene mutation. Clinical Dysmorphology, v. 16, n. 3, p. 163-166, 2007Tradução . . Disponível em: https://doi.org/10.1097/MCD.0b013e3280739753. Acesso em: 04 out. 2024.
APA
Ceide, R. M. Z., Guion-Almeida, M. L., Rodini, E. S. de O., Oliveira, N. A. de J., & Passos-Bueno, M. R. (2007). Hydrocephalus and moderate mental retardation in a boy with Van der Woude phenotype and IRF6 gene mutation. Clinical Dysmorphology, 16( 3), 163-166. doi:10.1097/MCD.0b013e3280739753
NLM
Ceide RMZ, Guion-Almeida ML, Rodini ES de O, Oliveira NA de J, Passos-Bueno MR. Hydrocephalus and moderate mental retardation in a boy with Van der Woude phenotype and IRF6 gene mutation [Internet]. Clinical Dysmorphology. 2007 ; 16( 3): 163-166.[citado 2024 out. 04 ] Available from: https://doi.org/10.1097/MCD.0b013e3280739753
Vancouver
Ceide RMZ, Guion-Almeida ML, Rodini ES de O, Oliveira NA de J, Passos-Bueno MR. Hydrocephalus and moderate mental retardation in a boy with Van der Woude phenotype and IRF6 gene mutation [Internet]. Clinical Dysmorphology. 2007 ; 16( 3): 163-166.[citado 2024 out. 04 ] Available from: https://doi.org/10.1097/MCD.0b013e3280739753
Artigo de periodico
Frontonasal dysplasia, neuronal migration error and lymphoedema of limbs (2004)
Lopes, Vera Lúcia Gil da Silva; Guion-Almeida, Maria Leine; Giffoni, Silvyo David Araújo
Source: Clinical Dysmorphology. Unidade: HRAC
Subjects: ANORMALIDADES CRANIOFACIAIS, ANORMALIDADES MÚLTIPLAS, DELEÇÃO DE GENES, LINFEDEMA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LOPES, Vera Lúcia Gil da Silva e GUION-ALMEIDA, Maria Leine e GIFFONI, Silvyo David Araújo. Frontonasal dysplasia, neuronal migration error and lymphoedema of limbs. Clinical Dysmorphology, v. 13, n. Ja 2004, p. 35-37, 2004Tradução . . Disponível em: https://doi.org/10.1097/00019605-200401000-00010. Acesso em: 04 out. 2024.
APA
Lopes, V. L. G. da S., Guion-Almeida, M. L., & Giffoni, S. D. A. (2004). Frontonasal dysplasia, neuronal migration error and lymphoedema of limbs. Clinical Dysmorphology, 13( Ja 2004), 35-37. doi:10.1097/00019605-200401000-00010
NLM
Lopes VLG da S, Guion-Almeida ML, Giffoni SDA. Frontonasal dysplasia, neuronal migration error and lymphoedema of limbs [Internet]. Clinical Dysmorphology. 2004 ; 13( Ja 2004): 35-37.[citado 2024 out. 04 ] Available from: https://doi.org/10.1097/00019605-200401000-00010
Vancouver
Lopes VLG da S, Guion-Almeida ML, Giffoni SDA. Frontonasal dysplasia, neuronal migration error and lymphoedema of limbs [Internet]. Clinical Dysmorphology. 2004 ; 13( Ja 2004): 35-37.[citado 2024 out. 04 ] Available from: https://doi.org/10.1097/00019605-200401000-00010

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