Hasil Pencarian - Miranda Di Biase

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  1. 1
    P434: An atypical presentation of Williams syndrome in a patient with a co-occurring FOXP4 likely pathogenic variant: A case report

    P434: An atypical presentation of Williams syndrome in a patient with a co-occurring FOXP4 likely pathogenic variant: A case report oleh Rebecca Abel, Miranda Di Biase

    Diterbitkan 2024-01-01
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  2. 2
    P119: Comparison of two cases with the same APC genotype and different phenotypes

    P119: Comparison of two cases with the same APC genotype and different phenotypes oleh Eva Spier, Miranda Di Biase

    Diterbitkan 2024-01-01
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  3. 3
    P318: Impact of genetic counseling using GUÍA on diverse families’ understanding of genomic results: Finding from the NYCKidSeq randomized controlled trial*

    P318: Impact of genetic counseling using GUÍA on diverse families’ understanding of genomic results: Finding from the NYCKidSeq randomized controlled trial* oleh Sabrina Suckiel, Nicole Kelly, Jacqueline Odgis, Katie Gallagher, Monisha Sebastin, Katherine Bonini, Priya Marathe, Kaitlyn Brown, Miranda Di Biase, Michelle Ramos, Jessica Rodriguez, Laura Scarimbolo, Beverly Insel, Randi Zinberg, George Diaz, John Greally, Noura Abul-Husn, Laurie Bauman, Carol Horowitz, Bruce Gelb, Melissa Wasserstein, Eimear Kenny

    Diterbitkan 2023-01-01
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  4. 4
    P245: GUÍA application: Effectiveness in enhancing communication of genomic results in diverse, multilingual populations*

    P245: GUÍA application: Effectiveness in enhancing communication of genomic results in diverse, multilingual populations* oleh Priya Marathe, Sabrina Suckiel, Jacqueline Odgis, Katie Gallagher, Monisha Sebastin, Katherine Bonini, Kaitlyn Brown, Miranda Di Biase, Nicole Kelly, Michelle Ramos, Jessica Rodriguez, Laura Scarimbolo, Beverly Insel, Randi Zinberg, George Diaz, John Greally, Noura Abul-Husn, Laurie Bauman, Carol Horowitz, Bruce Gelb, Melissa Wasserstein, Eimear Kenny

    Diterbitkan 2023-01-01
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  5. 5
    Evaluating parental personal utility of pediatric genetic and genomic testing in a diverse, multilingual population

    Evaluating parental personal utility of pediatric genetic and genomic testing in a diverse, multilingual population oleh Priya N. Marathe, Sabrina A. Suckiel, Katherine E. Bonini, Nicole R. Kelly, Laura Scarimbolo, Beverly J. Insel, Jacqueline A. Odgis, Monisha Sebastin, Michelle A. Ramos, Miranda Di Biase, Katie M. Gallagher, Kaitlyn Brown, Jessica E. Rodriguez, Nicole Yelton, Karla Lopez Aguiñiga, Michelle A. Rodriguez, Estefany Maria, Jessenia Lopez, Randi E. Zinberg, George A. Diaz, John M. Greally, Noura S. Abul-Husn, Laurie J. Bauman, Bruce D. Gelb, Melissa P. Wasserstein, Eimear E. Kenny, Carol R. Horowitz

    Diterbitkan 2024-07-01
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  6. 6
    The TeleKidSeq pilot study: incorporating telehealth into clinical care of children from diverse backgrounds undergoing whole genome sequencing

    The TeleKidSeq pilot study: incorporating telehealth into clinical care of children from diverse backgrounds undergoing whole genome sequencing oleh Monisha Sebastin, Jacqueline A. Odgis, Sabrina A. Suckiel, Katherine E. Bonini, Miranda Di Biase, Kaitlyn Brown, Priya Marathe, Nicole R. Kelly, Michelle A. Ramos, Jessica E. Rodriguez, Karla López Aguiñiga, Jessenia Lopez, Estefany Maria, Michelle A. Rodriguez, Nicole M. Yelton, Charlotte Cunningham-Rundles, Katie Gallagher, Thomas V. McDonald, Patricia E. McGoldrick, Mimsie Robinson, Arye Rubinstein, Lisa H. Shulman, Steven M. Wolf, Elissa Yozawitz, Randi E. Zinberg, Noura S. Abul-Husn, Laurie J. Bauman, George A. Diaz, Bart S. Ferket, John M. Greally, Vaidehi Jobanputra, Bruce D. Gelb, Carol R. Horowitz, Eimear E. Kenny, Melissa P. Wasserstein

    Diterbitkan 2023-03-01
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