Hasil Pencarian - Daniel Bellissimo

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  1. 1
    P082: Increased risk of hematolymphoid neoplasms in individuals with heterozygous deletion of a Fanconi anemia gene

    P082: Increased risk of hematolymphoid neoplasms in individuals with heterozygous deletion of a Fanconi anemia gene oleh Taimoor Sheikh, Abigail Peffer, Daniel Bellissimo, Mahmoud Aarabi, Svetlana Yatsenko

    Diterbitkan 2024-01-01
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  2. 2
    P424: An unusual recombinant chromosome 6 derived from a parental double paracentric inversion

    P424: An unusual recombinant chromosome 6 derived from a parental double paracentric inversion oleh Melanie Babcock, Emily Lancaster, Damara Ortiz, Daniel Bellissimo, Evan Powell, Svetlana Yatsenko

    Diterbitkan 2023-01-01
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  3. 3
    Case report: Early use of whole exome sequencing unveils HNRNPU-related neurodevelopmental disorder and answers additional clinical questions through reanalysis

    Case report: Early use of whole exome sequencing unveils HNRNPU-related neurodevelopmental disorder and answers additional clinical questions through reanalysis oleh Erika Nicole Dreikorn, Erika Nicole Dreikorn, Christine Munro, Christine Munro, Natasha Robin Berman, Natasha Robin Berman, Amina Kunovac, Daniel Bellissimo, Mylynda B. Massart

    Diterbitkan 2024-05-01
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  4. 4
    P257: A single institution analysis of in-house whole genome sequencing within pediatric and neonatal intensive care units (The PISCES Study)

    P257: A single institution analysis of in-house whole genome sequencing within pediatric and neonatal intensive care units (The PISCES Study) oleh Peter Nelson, Cate Walsh Vockley, Georgianne Arnold, Jirair Bedoyan, Amina Kunovac, Lindsey Kelly, Dara Kozak, Alexander Yatsenko, Jennifer Atkinson, Adrian Lee, Daniel Bellissimo, Jerry Vockley, Lina Ghaloul-Gonzalez

    Diterbitkan 2023-01-01
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