Torthaí cuardaigh - Danilo Moretti‐Ferreira

Beachtaigh na torthaí
  1. 1
    Genética e linguagem na síndrome de Williams-Beuren: uma condição neuro-cognitiva peculiar

    Genética e linguagem na síndrome de Williams-Beuren: uma condição neuro-cognitiva peculiar de réir Natalia Freitas Rossi, Danilo Moretti‐Ferreira, Célia Maria Giacheti

    Foilsithe / Cruthaithe 2006
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  2. 2
    Perfil comunicativo de indivíduos com a síndrome de Williams-Beuren

    Perfil comunicativo de indivíduos com a síndrome de Williams-Beuren de réir Natalia Freitas Rossi, Danilo Moretti‐Ferreira, Célia Maria Giacheti

    Foilsithe / Cruthaithe 2007
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    Artigo
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  3. 3
    Linguagem narrativa e fluência na síndrome de down: uma revisão

    Linguagem narrativa e fluência na síndrome de down: uma revisão de réir Marília Piazzi Seno, Célia Maria Giacheti, Danilo Moretti‐Ferreira

    Foilsithe / Cruthaithe 2014
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  4. 4
    Cytogenetic Evidence of Involvement of Chromosome Regions 15q12 and 12q15 in Conditions with Associated Overgrowth

    Cytogenetic Evidence of Involvement of Chromosome Regions 15q12 and 12q15 in Conditions with Associated Overgrowth de réir Anita Wajntal, Danilo Moretti‐Ferreira, Deise Helena de Souza, Célia Priszkulnik Koiffmann

    Foilsithe / Cruthaithe 1993
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  5. 5
    Sulcus vocalis: probable genetic etiology. Report of four cases in close relatives

    Sulcus vocalis: probable genetic etiology. Report of four cases in close relatives de réir Regina Helena Garcia Martins, Rafael Silva, Danilo Moretti‐Ferreira, Norimar Hernandes Dias

    Foilsithe / Cruthaithe 2007
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  6. 6
    Perfil da fluência da fala na síndrome de Williams-Beuren: estudo preliminar

    Perfil da fluência da fala na síndrome de Williams-Beuren: estudo preliminar de réir Natalia Freitas Rossi, Deise Helena de Souza, Danilo Moretti‐Ferreira, Célia Maria Giacheti

    Foilsithe / Cruthaithe 2009
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  7. 7
    Fluorescent in situ hybridization (FISH) as a diagnostic tool for Williams-Beuren syndrome

    Fluorescent in situ hybridization (FISH) as a diagnostic tool for Williams-Beuren syndrome de réir Deise Helena de Souza, Danilo Moretti‐Ferreira, Lígia Maria Suppo de Souza Rugolo

    Foilsithe / Cruthaithe 2007
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  8. 8
    Diagnosis of Smith-Lemli-Opitz syndrome by ultraviolet spectrophotometry

    Diagnosis of Smith-Lemli-Opitz syndrome by ultraviolet spectrophotometry de réir Fernanda B. Scalco, Vania M. Cruzes, R Vendramini, Iguatemy Lourenço Brunetti, Danilo Moretti‐Ferreira

    Foilsithe / Cruthaithe 2003
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  9. 9
    Gagueira desenvolvimental persistente familial: disfluências e prevalência

    Gagueira desenvolvimental persistente familial: disfluências e prevalência de réir Paula Roberta Nogueira, Cristiane Moço Canhetti de Oliveira, Célia Maria Giacheti, Danilo Moretti‐Ferreira

    Foilsithe / Cruthaithe 2015
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  10. 10
    X monosomy and balanced Robertsonian translocation in a girl with Turner Syndrome

    X monosomy and balanced Robertsonian translocation in a girl with Turner Syndrome de réir Aline Lourenço da Silva, Renata LL Ferreira de Lima, Lucilene Arilho Ribeiro, Danilo Moretti‐Ferreira

    Foilsithe / Cruthaithe 2006
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  11. 11
    MOMO syndrome associated with autism: a case report

    MOMO syndrome associated with autism: a case report de réir Carina Tatiana Giunco, Danilo Moretti‐Ferreira, A.E. Silva, Sandra Rocha, Agnes Cristina Fett‐Conte

    Foilsithe / Cruthaithe 2008
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  12. 12
    Smith-Lemli-Opitz syndrome: clinical and biochemical findings in Brazilian patients

    Smith-Lemli-Opitz syndrome: clinical and biochemical findings in Brazilian patients de réir Fernanda B. Scalco, Paulo Alberto Otto, Iguatemy Lourenço Brunetti, Vania M. Cruzes, Danilo Moretti‐Ferreira

    Foilsithe / Cruthaithe 2006
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  13. 13
    A rare karyotype presenting monosomy Xp and trisomy 17q in a patient with MCA/DI

    A rare karyotype presenting monosomy Xp and trisomy 17q in a patient with MCA/DI de réir Ingrid Nunes Volavicius, Deise Helena de Souza, Cátia Regina Branco da Fonseca, Danilo Moretti‐Ferreira

    Foilsithe / Cruthaithe 2018
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  14. 14
    Are variants in sex hormone metabolizing genes associated with stuttering?

    Are variants in sex hormone metabolizing genes associated with stuttering? de réir Carlos Eduardo Frigério Domingues, Katherine Grainger, Hui Cheng, Danilo Moretti‐Ferreira, Sheikh Riazuddin, Dennis Drayna

    Foilsithe / Cruthaithe 2019
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  15. 15
    Transmission analysis of candidate genes for nonsyndromic oral clefts in Brazilian parent-child triads with recurrence

    Transmission analysis of candidate genes for nonsyndromic oral clefts in Brazilian parent-child triads with recurrence de réir Aline Lourenço da Silva, Lucilene Arilho Ribeiro, Margaret E. Cooper, Mary L. Marazita, Danilo Moretti‐Ferreira

    Foilsithe / Cruthaithe 2006
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  16. 16
    Evaluation of the association between polymorphisms at the DRD2 locus and stuttering

    Evaluation of the association between polymorphisms at the DRD2 locus and stuttering de réir Changsoo Kang, Bianca Santos Domingues, Eduardo Sainz, Carlos Eduardo Frigério Domingues, Dennis Drayna, Danilo Moretti‐Ferreira

    Foilsithe / Cruthaithe 2011
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  17. 17
    Sulcus vocalis: evidence for autosomal dominant inheritance

    Sulcus vocalis: evidence for autosomal dominant inheritance de réir Regina Martins, Tatiana Maria Gonçalves, D.S. Neves, Thalita Fracalossi, Elaine Lara Mendes Tavares, Danilo Moretti‐Ferreira

    Foilsithe / Cruthaithe 2011
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  18. 18
    A rare non-Robertsonian translocation involving chromosomes 15 and 21

    A rare non-Robertsonian translocation involving chromosomes 15 and 21 de réir Marcelo Razera Baruffi, Deise Helena de Souza, Rosana Aparecida Bicudo Silva, Ester Silveira Ramos, Danilo Moretti‐Ferreira

    Foilsithe / Cruthaithe 2013
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  19. 19
    Short Communication Assessment of clinical scoring systems for the diagnosis of Williams-Beuren syndrome

    Short Communication Assessment of clinical scoring systems for the diagnosis of Williams-Beuren syndrome de réir D.E.S. Leme, Deise Helena de Souza, Graciela Mercado, E.A. Pastene, Adriano Días, Danilo Moretti‐Ferreira

    Foilsithe / Cruthaithe 2013
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  20. 20
    Search for Genomic Alterations in Monozygotic Twins Discordant for Cleft Lip and/or Palate

    Search for Genomic Alterations in Monozygotic Twins Discordant for Cleft Lip and/or Palate de réir Jane W. Kimani, Koh-ichiro Yoshiura, Min Shi, Astanand Jugessur, Danilo Moretti‐Ferreira, Kaare Christensen, Jeffrey C. Murray

    Foilsithe / Cruthaithe 2009
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