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

Detalles Bibliográficos
Autores principales:	Lyon, Sarah M., Israel, Jacqueline S., Farmer, Rebecca L., Berres, Mark, Pavelec, Derek M., Poore, Samuel O., Siebert, John W.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Lippincott Williams & Wilkins 2022
Materias:	EPoster Resident Competition
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8984417/ http://dx.doi.org/10.1097/01.GOX.0000828264.23483.82

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