Ngā hua rapu - Danilo Moretti‐Ferreira

Whakamahine hua
  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 mā Natalia Freitas Rossi, Danilo Moretti‐Ferreira, Célia Maria Giacheti

    I whakaputaina 2006
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Revisão
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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 mā Natalia Freitas Rossi, Danilo Moretti‐Ferreira, Célia Maria Giacheti

    I whakaputaina 2007
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    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 mā Marília Piazzi Seno, Célia Maria Giacheti, Danilo Moretti‐Ferreira

    I whakaputaina 2014
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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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 mā Anita Wajntal, Danilo Moretti‐Ferreira, Deise Helena de Souza, Célia Priszkulnik Koiffmann

    I whakaputaina 1993
    Whiwhi kuputuhi katoa
    Artigo
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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 mā Regina Helena Garcia Martins, Rafael Silva, Danilo Moretti‐Ferreira, Norimar Hernandes Dias

    I whakaputaina 2007
    Whiwhi kuputuhi katoa
    Artigo
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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 mā Natalia Freitas Rossi, Deise Helena de Souza, Danilo Moretti‐Ferreira, Célia Maria Giacheti

    I whakaputaina 2009
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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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 mā Deise Helena de Souza, Danilo Moretti‐Ferreira, Lígia Maria Suppo de Souza Rugolo

    I whakaputaina 2007
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  8. 8
    Diagnosis of Smith-Lemli-Opitz syndrome by ultraviolet spectrophotometry

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

    I whakaputaina 2003
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  9. 9
    Gagueira desenvolvimental persistente familial: disfluências e prevalência

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

    I whakaputaina 2015
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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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 mā Aline Lourenço da Silva, Renata LL Ferreira de Lima, Lucilene Arilho Ribeiro, Danilo Moretti‐Ferreira

    I whakaputaina 2006
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  11. 11
    MOMO syndrome associated with autism: a case report

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

    I whakaputaina 2008
    Whiwhi kuputuhi katoa
    Artigo
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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 mā Fernanda B. Scalco, Paulo Alberto Otto, Iguatemy Lourenço Brunetti, Vania M. Cruzes, Danilo Moretti‐Ferreira

    I whakaputaina 2006
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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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 mā Ingrid Nunes Volavicius, Deise Helena de Souza, Cátia Regina Branco da Fonseca, Danilo Moretti‐Ferreira

    I whakaputaina 2018
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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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? mā Carlos Eduardo Frigério Domingues, Katherine Grainger, Hui Cheng, Danilo Moretti‐Ferreira, Sheikh Riazuddin, Dennis Drayna

    I whakaputaina 2019
    Whiwhi kuputuhi katoa
    Carta
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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 mā Aline Lourenço da Silva, Lucilene Arilho Ribeiro, Margaret E. Cooper, Mary L. Marazita, Danilo Moretti‐Ferreira

    I whakaputaina 2006
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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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 mā Changsoo Kang, Bianca Santos Domingues, Eduardo Sainz, Carlos Eduardo Frigério Domingues, Dennis Drayna, Danilo Moretti‐Ferreira

    I whakaputaina 2011
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Carta
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  17. 17
    Sulcus vocalis: evidence for autosomal dominant inheritance

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

    I whakaputaina 2011
    Whiwhi kuputuhi katoa
    Artigo
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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 mā Marcelo Razera Baruffi, Deise Helena de Souza, Rosana Aparecida Bicudo Silva, Ester Silveira Ramos, Danilo Moretti‐Ferreira

    I whakaputaina 2013
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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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 mā D.E.S. Leme, Deise Helena de Souza, Graciela Mercado, E.A. Pastene, Adriano Días, Danilo Moretti‐Ferreira

    I whakaputaina 2013
    Whiwhi kuputuhi katoa
    Artigo
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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 mā Jane W. Kimani, Koh-ichiro Yoshiura, Min Shi, Astanand Jugessur, Danilo Moretti‐Ferreira, Kaare Christensen, Jeffrey C. Murray

    I whakaputaina 2009
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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