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MCL Molecular Genetics Congenital Inherited Diseases Patient Information MC123597
MCL Molecular Genetics Congenital Inherited Diseases Patient Information Complete print Reset Form Molecular Genetics Congenital Inherited Diseases Patient Information Instructions accurate interpretation reporting genetic
MCL Familial Mutation Testing Required Patient Information MC1235202
MCL Familial Mutation Testing Required Patient Information Complete print Familial Variant Testing Required Patient Information Reset Form Instructions accurate interpretation reporting genetic results
MCL - Final Disposition of Fetal/Stillborn Remains - MC1235-228
MCL - Final Disposition Fetal/Stillborn Remains - Final Disposition Fetal Stillborn Remains Date mm dd yyyy understand signing Clinic dispose
MCL First TrimesterSequential Maternal Screening Patient Information MC1235122
MCL TrimesterSequential Maternal Screening Patient Information Complete print Reset Form Trimester Sequential Maternal Screening Patient Information Patient Information Middle Birth Date
MCL Molecular Genetics Prenatal Patient Information MC1235306
MCL Molecular Genetics Prenatal Patient Information Complete print Molecular Genetics Prenatal Patient Information Reset Form Instructions accurate interpretation reporting genetic results
MCL Erythrocytosis Patient Information MC1235177
MCL Erythrocytosis Patient Information Complete print Reset Form Erythrocytosis Patient Information Instructions accurate interpretation reporting results contingent
MCL - Bone Histomorphometry Patient Information - MC1235-59
MCL - Bone Histomorphometry Patient Information - Complete print Bone Histomorphometry Patient Information Reset Form Patient Information Patient Middle Referring Provider
MCL Nerve Biopsy Patient Information MC123590
MCL Nerve Biopsy Patient Information Complete print Reset Form Nerve Biopsy Patient Information Instructions information completed copy
MCL Molecular Genetics Hereditary Custom Gene Panel Patient Information MC1235282
MCL Molecular Genetics Hereditary Custom Gene Panel Patient Information Complete print Reset Form Molecular Genetics Hereditary Custom Gene Panel Patient Information Instructions accurate interpretation reporting
MCL Biochemical Genetics Patient Information MC1235116
MCL Biochemical Genetics Patient Information Complete print Reset Form Biochemical Genetics Patient Information Complete information Send paperwork specimen return
MCL Hematopathology Patient Information MC1235175
MCL Hematopathology Patient Information Complete print Reset Form Hematopathology Patient Information Instructions Send paperwork pathology test reports
MCL Platelet Antibody Screen Serum Information MC1235242
MCL Platelet Antibody Screen Serum Information Complete print Platelet Antibody Screen Serum Patient Information Reset Form Patient Information Patient Middle Birth Date
nt_crl_data_for_first_trimester_sequential_maternal_screening.pdf
Client Information MCL Account Number Account Name Contact Phone Street Address City State ZIP Code MCL will provide sonographer QC data on a regular basis. Select one of the following: Client agrees to distribute QC data to the...
MCL Molecular Genetics Biochemical Disorders Patient Information MC1235100
MCL Molecular Genetics Biochemical Disorders Patient Information Complete print Reset Form Molecular Genetics Biochemical Disorders Patient Information Instructions accurate interpretation reporting genetic results
MCL Inborn Errors Immunity Autoimmunity Autoinflammatory Disease Patient Information Complete print Reset Form Inborn Errors Immunity Autoimmunity Autoinflammatory Disease Patient Information Instructions Accurate interpretation reporting
MCL Chimerism Analysis Information MC1235124
MCL Chimerism Analysis Information Complete print Reset Form Chimerism Analysis Information separate form specimen submitted Note results
MCL Molecular Genetics Patient Information for Uniparental Disomy MC1235300
MCL Molecular Genetics Patient Information Uniparental Disomy Complete print Reset Form Molecular Genetics Uniparental Disomy Patient Information Instructions Accurate interpretation reporting genetic results
MCL ThalassemiaHemoglobinopathy Patient Information MC123536
MCL ThalassemiaHemoglobinopathy Patient Information Complete print Thalassemia Hemoglobinopathy Patient Information Reset Form Instructions information requested important interpretation test
MCL Chromosomal Microarray Testing Patient Information MC1235166
MCL Chromosomal Microarray Testing Patient Information Complete print Chromosomal Microarray Patient Information Instructions accurate interpretation reporting genetic results contingent
MCL GATA2 Gene Sequencing Patient Information MC1235249
MCL GATA2 Gene Sequencing Patient Information Complete print GATA2 Gene Sequencing Patient Information Reset Form Instructions accurate interpretation reporting genetic results
MCL Familial Chromosomal Microarray FISH Testing Information MC1235236
MCL Familial Chromosomal Microarray FISH Testing Information Family Member Phenotype Information Genomic Testing Instructions accurate interpretation reporting familial genetic results highly contingent
MCL Molecular Genetics Neurology Patient Information MC1235235
MCL Molecular Genetics Neurology Patient Information Complete print Molecular Genetics Neurology Patient Information Reset Form Instructions accurate interpretation reporting genetic results
MCL UGT1A1 Gene Testing Patient Information MC1235165
MCL UGT1A1 Gene Testing Patient Information Complete print UGT1A1 Gene Testing Patient Information Reset Form Instructions accurate interpretation reporting genetic results
MCL Hereditary Renal Genetic Testing Patient Information Form MC1235292
MCL Hereditary Renal Genetic Testing Patient Information Form Complete print Hereditary Renal Genetic Testing Patient Information Reset Form Instructions accurate interpretation reporting genetic
MCL Viral Susceptibility Lymphoproliferation Hemophagocytic Lymphohistiocytosis Patient Information Complete print Reset Form Viral Susceptibility Lymphoproliferation Hemophagocytic Lymphohistiocytosis Patient Information Instructions...
MCL Brutons Tyrosine Kinase BTK Genotype Patient Information MC1235132
MCL Brutons Tyrosine Kinase BTK Genotype Patient Information Complete print Bruton Tyrosine Kinase BTK Gene Sequencing Patient Information Reset Form Instructions accurate interpretation reporting
MCL Molecular Hematopathology Patient Information MC1235189
MCL Molecular Hematopathology Patient Information Complete print Reset Form Molecular Hematopathology Patient Information Cell Chronic Lymphocytic Leukemia CLL IGVH TP53
mc1235-69-lead-and-heavy-metals-reporting-spanish.pdf
T956 ©2023 Mayo Foundation for Medical Education and Research MC1235-69SPrev0823 Informes sobre plomo y metales pesados Lead and Heavy Metals Reporting (Spanish) Page 1 of 2 La siguiente información debe ser proporcionada para todas las...
MCL Rare Coagulation Disorder Patient Information MC1235264
MCL Rare Coagulation Disorder Patient Information Complete print Reset Form Rare Coagulation Disorder Patient Information Instructions Genetic testing rare hereditary disorders blood coagulation
MCL - Informed Consent for Genetic Testing for Deceased Individuals - MC1235-243
MCL - Informed Consent Genetic Testing Deceased Individuals - Informed Consent Genetic Testing Deceased Individuals Testing genetic conditions complex Prior providing consent
MCL Request for Original Newborn Screening Card MC1235156
MCL Request Original Newborn Screening Card Complete print submit Request Original Newborn Screening Card Reset Form State Newborn Screening Laboratory Address Street
MCL Von Willebrand Disease Patient Information MC1235265
MCL Von Willebrand Disease Patient Information Complete print Reset Form von Willebrand Disease Patient Information Instructions von Willebrand factor VWF gene testing von Willebrand
MCL Lead and Heavy Metals Reporting MC123569
MCL Lead Heavy Metals Reporting Complete print Lead Heavy Metals Reporting Reset Form information Lead
MCL GynCytology Patient Information MC1235129
MCL GynCytology Patient Information Complete print Reset Form Gyn Cytology Patient Information Instructions Send completed copy form specimen
MCL Epidermal Nerve Fiber Density Patient Information MC1235179
MCL Epidermal Nerve Fiber Density Patient Information Complete print Epidermal Nerve Fiber Density Patient Information Reset Form Instructions provide service supply
MCL Multiple Genotype Test List MC409194
MCL Multiple Genotype Test List Multiple Genotype Test List Instructions tests performed single blood EDTA specimen
Creepy, Dreadful, Wonderful Viruses - Insights
PACE / State of FLIn this month’s “Virtual Lecture” Bobbi Pritt, M.D., shares a series of spooky tales to scare and amaze related to the discovery, characterization, and clinical presentation of notable viruses.
MCLRequest for Supplies MC0748
MCLRequest Supplies Complete print Request Supplies Reset Form Client Information required Client Account Number Client Contact Phone Date
MCL Downtime Form Downtime Form Clinic Laboratories Attn Dr William Morice II 3050 Superior Drive NW Rochester MN 55905 Fax
fabry_disease_testing_algorithm.pdf
© Mayo Foundation for Medical Education and Research (MFMER). All rights reserved. 06/2024 Fabry Disease Diagnostic Testing Algorithm FMTT / Familial Variant, Targeted Testing, Varies Clinical suspicion or family history of Fabry...
ulcerative-colitis-crohn-disease-therapeutic-drug-monitoring-algorithm.pdf
No enzyme activity Thiopurine therapy contraindicated Decreased enzyme activity Reduced thiopurine dosing appropriate Normal enzyme activity Appropriate for weight-based dosing Diagnosis of ulcerative colitis (UC) or Crohn disease...
newborn_screen_follow-up_for_mucopolysaccharidosis_type_i.pdf
© Mayo Foundation for Medical Education and Research (MFMER). All rights reserved. 03/2024 Newborn screen result: decreased alpha-L-iduronidase (IDUA) Order 1 from each of the following groups: ■ IDUAW / Alpha-L-Iduronidase,...
porphyria__acute__testing_algorithm.pdf
© Mayo Foundation for Medical Education and Research (MFMER). All rights reserved. 05/2024 Porphyria (Acute) Testing Algorithm Decreased ALAD activity Normal ALAD activity Isolated ALA increase Confirms ADP Consider CGPH / Custom Gene...
glucose-6-phosphate-dehydrogenase-deficiency-diagnostic-algorithm.pdf
© Mayo Foundation for Medical Education and Research (MFMER). All rights reserved. Glucose-6-Phosphate Dehydrogenase (G6PD) Deficiency Diagnostic Algorithm * If patient status is post-allogeneic stem cell transplant (HSCT), testing can...
tp53_mutation_testing_algorithm.pdf
© Mayo Foundation for Medical Education and Research (MFMER). All rights reserved. 04/2023 Patient diagnosed with either chronic lymphocytic leukemia (CLL) or a lymphoid or hematologic neoplasm other than CLL Patient diagnosed with...
newborn-screen-follow-up-elevated-c14-long-chain-acylcarnitine.pdf
© Mayo Foundation for Medical Education and Research (MFMER). All rights reserved. 06/2023 Newborn screen result: Elevated C14:1 with possible elevations of other long-chain acylcarnitine Perform: Plasma ammonia, blood gas, glucose,...
platelet_antibody_algorithm.pdf
© Mayo Foundation for Medical Education and Research (MFMER). All rights reserved. 05/2024 Platelet Antibody Testing Algorithm Autoimmune cause of thrombocytopenia suspected, such as: ■ Idiopathic thrombocytopenia purpura (ITP) ■ Secondary...
12/2019© Mayo Foundation for Medical Education and Research (MFMER). All rights reserved. NOYES Alpha1 Antitrypsin—A Comprehensive Testing Algorithm A1AT serum level and proteotype Order A1ALC / Alpha-1-Antitrypsin Proteotype S/Z by...
newborn-screen-follow-up-elevated-c4-oh-acylcarnitine.pdf
© Mayo Foundation for Medical Education and Research (MFMER). All rights reserved. 09/2023 Newborn screen result: Elevated C4-OH acylcarnitine Perform: Plasma ammonia, blood gas, glucose, electrolytes Order: ■ OAU / Organic Acids Screen,...
laboratory_approach_to_the_diagnosis_of_amyloidosis.pdf
04/2024© Mayo Foundation for Medical Education and Research (MFMER). All rights reserved. Amyloidosis: Laboratory Approach to Diagnosis Possible patient presentations: ■ Nephrotic-range proteinuria with or without renal insufficiency...