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

oleh: Sarah M. Lyon, MD, Jacqueline S. Israel, MD, Rebecca L. Farmer, MD, Mark Berres, PhD, Derek M. Pavelec, PhD, Samuel O. Poore, MD PhD, John W. Siebert, MD

Format: Article
Diterbitkan: Wolters Kluwer 2022-04-01

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