Hakutulokset - Daniel Bellissimo

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

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

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P725: Clinical exome sequencing towards molecular diagnosis: Insights and outcomes from 822 pediatric cases Tekijä Yinghong Pan, Patrick Danley, Tamar Kramer, Karen Buser, Mehrdad Noruzinia, Alexander Yatsenko, Daniel Bellissimo, Fen Guo

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

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P257: A single institution analysis of in-house whole genome sequencing within pediatric and neonatal intensive care units (The PISCES Study) Tekijä 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

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