检索结果 - Danilo Moretti‐Ferreira

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  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 由 Natalia Freitas Rossi, Danilo Moretti‐Ferreira, Célia Maria Giacheti

    出版 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 由 Natalia Freitas Rossi, Danilo Moretti‐Ferreira, Célia Maria Giacheti

    出版 2007
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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 由 Marília Piazzi Seno, Célia Maria Giacheti, Danilo Moretti‐Ferreira

    出版 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 由 Anita Wajntal, Danilo Moretti‐Ferreira, Deise Helena de Souza, Célia Priszkulnik Koiffmann

    出版 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 由 Regina Helena Garcia Martins, Rafael Silva, Danilo Moretti‐Ferreira, Norimar Hernandes Dias

    出版 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 由 Natalia Freitas Rossi, Deise Helena de Souza, Danilo Moretti‐Ferreira, Célia Maria Giacheti

    出版 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 由 Deise Helena de Souza, Danilo Moretti‐Ferreira, Lígia Maria Suppo de Souza Rugolo

    出版 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 由 Fernanda B. Scalco, Vania M. Cruzes, R Vendramini, Iguatemy Lourenço Brunetti, Danilo Moretti‐Ferreira

    出版 2003
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  9. 9
    Gagueira desenvolvimental persistente familial: disfluências e prevalência

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

    出版 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 由 Aline Lourenço da Silva, Renata LL Ferreira de Lima, Lucilene Arilho Ribeiro, Danilo Moretti‐Ferreira

    出版 2006
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  11. 11
    MOMO syndrome associated with autism: a case report

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

    出版 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 由 Fernanda B. Scalco, Paulo Alberto Otto, Iguatemy Lourenço Brunetti, Vania M. Cruzes, Danilo Moretti‐Ferreira

    出版 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 由 Ingrid Nunes Volavicius, Deise Helena de Souza, Cátia Regina Branco da Fonseca, Danilo Moretti‐Ferreira

    出版 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? 由 Carlos Eduardo Frigério Domingues, Katherine Grainger, Hui Cheng, Danilo Moretti‐Ferreira, Sheikh Riazuddin, Dennis Drayna

    出版 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 由 Aline Lourenço da Silva, Lucilene Arilho Ribeiro, Margaret E. Cooper, Mary L. Marazita, Danilo Moretti‐Ferreira

    出版 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 由 Changsoo Kang, Bianca Santos Domingues, Eduardo Sainz, Carlos Eduardo Frigério Domingues, Dennis Drayna, Danilo Moretti‐Ferreira

    出版 2011
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  17. 17
    Sulcus vocalis: evidence for autosomal dominant inheritance

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

    出版 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 由 Marcelo Razera Baruffi, Deise Helena de Souza, Rosana Aparecida Bicudo Silva, Ester Silveira Ramos, Danilo Moretti‐Ferreira

    出版 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 由 D.E.S. Leme, Deise Helena de Souza, Graciela Mercado, E.A. Pastene, Adriano Días, Danilo Moretti‐Ferreira

    出版 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 由 Jane W. Kimani, Koh-ichiro Yoshiura, Min Shi, Astanand Jugessur, Danilo Moretti‐Ferreira, Kaare Christensen, Jeffrey C. Murray

    出版 2009
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