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Mayo Clinic Laboratory and Pathology Research Roundup: March 5 - Insights

clinically as pathogenic or likely pathogenic are predominantly located in the region encoding the C-terminal DNA binding domain (DBD). We report on functional evaluation of the influence of 462 BRCA2...

newborn-screen-elevated-c16-c18-acylcarnitine.pdf

© Mayo Foundation for Medical Education and Research (MFMER). All rights reserved. 08/2023 Newborn screen result: ■ Elevated C16 acylcarnitine ■ Possible elevated 18:1 acylcarnitine Perform: Plasma ammonia, blood gas, glucose, electrolytes,...

newborn-screen-follow-up-elevated-c3-isolated.pdf

05/2023© Mayo Foundation for Medical Education and Research (MFMER). All rights reserved. Newborn Screen Follow-up for Isolated Elevation of C3 Newborn screen result: Isolated elevation of propionylcarnitine (C3) Perform: Plasma ammonia,...

MCL Hereditary Dyslipidemia Patient Information MC1235295

MCL Hereditary Dyslipidemia Patient Information Complete print Reset Form Hereditary Dyslipidemia Patient Information Instructions Accurate interpretation reporting genetic results contingent

newborn-screen-follow-up-elevated-leucine-algorithm.pdf

© Mayo Foundation for Medical Education and Research (MFMER). All rights reserved. 04/2025 Newborn screen result: Elevated leucine Perform urine ketones Order both of the following: ■ AAQP / Amino Acids, Quantitative, Plasma ■ OAU /...

Perspectives from Washington, D.C.: Bill Morice, M.D., Ph.D. - Insights

In this episode of “Answers From the Lab,” host Bobbi Pritt, M.D., chair of the Department of Laboratory Medicine and Pathology at Mayo Clinic, is joined by William Morice II, M.D., Ph.D., CEO and president of Mayo Clinic Laboratories. They...

glucose-6-phosphate-dehydrogenase-genotyping-interpretive-algorithm.pdf

In the following situations, order G6PDZ / Glucose-6-Phosphate Dehydrogenase (G6PD) Full Gene Sequencing: ■ To determine carrier status (female patient) or affected status (male patient) ■ Previous G6PD enzyme test result is...

MCL Primary Ciliary Dyskinesia Genetic Testing Patient Information MC1235297

MCL Primary Ciliary Dyskinesia Genetic Testing Patient Information Complete print Reset Form Primary Ciliary Dyskinesia Genetic Testing Patient Information Instructions Accurate interpretation reporting genetic results

MCL - Immunohistochemical (IHC)/In Situ Hybridization (ISH) Stains Request Form - MC0767-09A

MCL - Immunohistochemical (IHC)/In Situ Hybridization (ISH) Stains Request Form

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