Syndromic craniosynostosis associated with microdeletion of chromosome 19p13.12–19p13.2

por Lyon, Sarah M., Waggoner, Darrel, Halbach, Sara, Thorland, Erik C., Khorasani, Leila, Reid, Russell R.
Publicado 2015

PC3. IDENTIFICATION OF GENETIC VARIANTS IN PARRY ROMBERG DISEASE USING WHOLE EXOME SEQUENCING

por Lyon, Sarah M., Israel, Jacqueline S., Farmer, Rebecca L., Berres, Mark, Pavelec, Derek M., Poore, Samuel O., Siebert, John W.
Publicado 2022

Abstract 181: The Regenerative Effects Of Reconstruction: An Analysis Of Cutaneous Gene Expression Changes In Irradiated Breast Reconstruction Patients

por Gunderson, Kirsten A., Farmer, Rebecca L., Lyon, Sarah M., Israel, Jacqueline S., BonDurant, Sandra Splinter, Gast, Katherine M., Poore, Samuel O., Siebert, John W.
Publicado 2020