Factors associated with parental knowledge of neurofibromatosis type 1 (NF1): Parental affected status and genetic counseling von Solem, Emily P., Primiano, Michelle, McQuillen, Marshall P., Zak Goelz, Monika

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Clinical diagnosis of neurofibromatosis type I in multiple family members due to cosegregation of a unique balanced translocation with disruption of the NF1 locus: Testing consider... von Smith, Rebecca B., Solem, Emily P., Metz, Emma C., Wheeler, Ferrin C., Phillips, John A., Yenamandra, Ashwini

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A novel, likely pathogenic variant in UBTF‐related neurodegeneration with brain atrophy is associated with a severe divergent neurodevelopmental phenotype von Tinker, Rory J., Guess, Tiffany, Rinker, David C., Sheehan, Jonathan H., Lubarsky, Daniel, Porath, Binu, Mosera, Mackenzie, Mayo, Ping, Solem, Emily, Lee, Laura A., Sharam, Asha, Brault, Jennifer

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eP417: Exome sequencing unravels dual diagnoses and complex molecular etiologies in a family with prior negative diagnostic testing von Wheeler, Ferrin, Mosera, Mackenzie, Solem, Emily, Porath, Binu, Lee, Laura, Stricker, Thomas, Phillips, James, Phillips, John

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Abstract 15689: Ablation for Atrial Fibrillation in Patients With Rare Pathogenic Variants in Cardiomyopathy and Arrhythmia Genes von El-Harasis, Majd A, Yoneda, Zachary, Anderson, Katherine, Ye, Fei, Quintana, Joseph, Martinez-Parachini, Jose R, Jackson, Gregory, Varghese, Bibin, Crawford, Diane, Sun, Lili, Williams, Hollie L, O'Neill, Matthew, Davogustto, Giovanni E, Laws, James L, Murphy, Brittany, Tomasek, Kelsey, Su, Yan Ru, Solem, Emily, Metz, Emma, Smith, Carly, Stubbs, Douglas, Grauherr, Dakota, Wells, Quinn, Michaud, Gregory, saavedra, pablo, Estrada, Juan C, Richardson, Travis, Shen, Sharon, Kanagasundram, Arvindh, Montgomery, Jay A, Tandri, Harikrishna, Ellis, Christopher R, Crossley, George H, Kannankeril, Prince, Stevenson, Lynne W, Stevenson, William G, Lubitz, Steven A, Ellinor, Patrick T, Roden, Dan M, Shoemaker, Ben B

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55. A familial clinical presentation of neurofibromatosis type 1 co-segregates with a unique chromosomal abnormality von Smith, Rebecca, Solem, Emily, Metz, Emma, Duncan, Laura, Wheeler, Ferrin, Phillips, John, Yenamandra, Ashwini

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Data for Campus SLL von Ruimin, Ke, Weidner Jeffrey, Raheem Adeeba, Cheu Kelvin, Azfar Talha, Littles Angelica, Guilien Francisco, Solem Emily, Edens Christopher

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Clinical diagnosis of neurofibromatosis type I in multiple family members due to cosegregation of a unique balanced translocation with disruption of the NF1 locus: Testing consider... von Smith, Rebecca B, Solem, Emily P, Metz, Emma C, Wheeler, Ferrin C, Phillips, John A, Yenamandra, Ashwini

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