Addressing the Burdens That Newborn Screening Imposes on Underserved Communities by Strenk, Meghan E., Berrios, Courtney, Garrett, Jeremy R.

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Recurrent ACADVL molecular findings in individuals with a positive newborn screen for very long chain acyl-coA dehydrogenase (VLCAD) deficiency in the United States by Miller, Marcus J., Burrage, Lindsay C., Gibson, James B., Strenk, Meghan E., Lose, Edward J., Bick, David P., Elsea, Sarah H., Sutton, V. Reid, Sun, Qin, Graham, Brett H., Craigen, William J., Zhang, Victor Wei, Wong, Lee-Jun C.

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Diagnosis of mitochondrial disorders by concomitant next-generation sequencing of the exome and mitochondrial genome by Dinwiddie, Darrell L., Smith, Laurie D., Miller, Neil A., Atherton, Andrea M., Farrow, Emily G., Strenk, Meghan E., Soden, Sarah E., Saunders, Carol J., Kingsmore, Stephen F.

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Importance of cell wall mannoproteins for septum formation in Saccharomyces cerevisiae by Schmidt, Martin, Strenk, Meghan E., Boyer, Michael P., Fritsch, Bryan J.

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Disclosure of Misattributed Paternity by Prero, Moshe Y, Strenk, Meghan, Garrett, Jeremy, Kessler, Ann, Fanaroff, Jonathan M, Lantos, John D

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Developing a community-led rare disease ELSI research agenda by Berrios, Courtney, McBeth, Macy, Bradley-Ewing, Andrea, Schuetz, Nikolaus, Campbell, Annette, Talebizadeh, Zohreh, Garrett, Jeremy R, Falicov, Tamara, Martinez, Francisco, Hurley, Emily A

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eP033 - Improving the performance of newborn screening for mucopolysaccharidosis type II with second tier biomarker testing by Peck, Dawn, White, Amy, Pino, Gisele, Studinski, April, Strenk, Meghan, Gadea, Randi, Gannon, Jennifer, Heese, Bryce, Font-Montgomery, Esperanza, Klug, Tracy, Burton, Jennifer, Hoganson, George, Oglesbee, Devin, Gavrilov, Dimitar, Matern, Dietrich, Raymond, Kimiyo, Rinaldo, Piero, Tortorelli, Silvia

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eP028 - The role of biomarkers for the follow up of infants with positive newborn screening results for Fabry disease by Pino, Gisele, Studinski, April, White, Amy, Peck, Dawn, Minnich, Sara, Gadea, Randi, Strenk, Meghan, Gannon, Jennifer, Heese, Bryce, Font-Montgomery, Esperanza, Hamm, Austin, Dennis, Anna, Viall, Sarah, Gavrilov, Dimitar, Tortorelli, Silvia, Oglesbee, Devin, Rinaldo, Piero, Matern, Dietrich, Raymond, Kimiyo

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The role of biomarkers for the follow up of infants with positive newborn screening results for Fabry disease by Pino, Gisele, Studinski, April, White, Amy, Peck, Dawn, Minnich, Sara, Gadea, Randi, Strenk, Meghan, Gannon, Jennifer, Heese, Bryce, Font-Montgomery, Esperanza, Hamm, Austin, Dennis, Anna, Viall, Sarah, Gavrilov, Dimitar, Tortorelli, Silvia, Oglesbee, Devin, Rinaldo, Piero, Matern, Dietrich, Raymond, Kimiyo

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Improving the performance of newborn screening for mucopolysaccharidosis type II with second tier biomarker testing by Peck, Dawn, White, Amy, Pino, Gisele, Studinski, April, Strenk, Meghan, Gadea, Randi, Gannon, Jennifer, Heese, Bryce, Font-Montgomery, Esperanza, Klug, Tracy, Burton, Jennifer, Hoganson, George, Oglesbee, Devin, Gavrilov, Dimitar, Matern, Dietrich, Raymond, Kimiyo, Rinaldo, Piero, Tortorelli, Silvia

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Proximal microdeletions and microduplications of 1q21.1 contribute to variable abnormal phenotypes by Rosenfeld, Jill A, Traylor, Ryan N, Schaefer, G Bradley, McPherson, Elizabeth W, Ballif, Blake C, Klopocki, Eva, Mundlos, Stefan, Shaffer, Lisa G, Aylsworth, Arthur S

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