Hasil Pencarian - Jessica Scott Schwoerer
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P526: Insurance access to genetic testing: Experiences in the Midwest oleh April Hall, Jessica Scott Schwoerer
Diterbitkan 2024-01-01
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Rhabdomyolysis in a neonate due to very long chain acyl CoA dehydrogenase deficiency oleh Jessica Scott Schwoerer, Gena Cooper, Sandra van Calcar
Diterbitkan 2015-06-01
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Long-term outcomes in Amish patients diagnosed with propionic acidemia oleh Jessica Scott Schwoerer, Sarah Clowes Candadai, Patrice K. Held
Diterbitkan 2018-09-01
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Genotypes of patients with phenylalanine hydroxylase deficiency in the Wisconsin Amish oleh Jessica Scott Schwoerer, Nicoletta Drilias, Ashley Kuhl, Sean Mochal, Mei Baker
Diterbitkan 2018-06-01
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P556: Genetic providers’ views on trauma-informed care in genetics clinics oleh Amy Gaviglio, Kelsey Sala Hamrick, Jessica Scott Schwoerer, Loan Stone, Kaitlin Justice, Mathew Edick
Diterbitkan 2024-01-01
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Computational structural genomics and clinical evidence suggest BCKDK gain‐of‐function may cause a potentially asymptomatic maple syrup urine disease phenotype oleh Emily Singh, Young‐In Chi, Jessica Kopesky, Michael Zimmerman, Raul Urrutia, Donald Basel, Jessica Scott Schwoerer
Diterbitkan 2024-05-01
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