What follows is from The All ARUP Consult Genetics Content.
All ARUP Consult Genetics Content 1p/19q Deletion in Oligodendrogliomas Neurology Oncology 21-Hydroxylase Deficiency Congenital Adrenal Hyperplasia – 21-OHD CAH Endocrinology Nephrology and Urology Acute Lymphoblastic Leukemia – ALL Hematology Oncology Acute Lymphoblastic Leukemia FISH Panels Hematology Oncology Acute Myeloid Leukemia – AML Hematology Oncology Acute Myeloid Leukemia Mutation Panel by Next Generation Sequencing Hematology Oncology Alloimmune Hemolytic Disease of the Fetus and Newborn (RhCc, RhEe, RhD, or Kell Antigen Genotyping) Hematology Immunology Alpha Thalassemia Hematology Alpha-1-Antitrypsin Deficiency Testing Cardiology and Pulmonology Gastroenterology Alpha-Iduronidase Enzyme Activity in Leukocytes Metabolic and Mitochondrial Disorders Alport Syndrome Panel, Sequencing and Deletion/Duplication Gastroenterology Nephrology and Urology Alzheimer’s Disease Neurology Amenorrhea Reproductive Health and Infertility Amenorrhea Testing Algorithm Reproductive Health and Infertility Angelman Syndrome and Prader-Willi Syndrome Developmental Delay and Intellectual Disability Neurology Angelman Syndrome and Prader-Willi Syndrome by Methylation-Specific MLPA Developmental Delay and Intellectual Disability Neurology Ankylosing Spondylitis (HLA-B27) Genotyping Musculoskeletal and Connective Tissue Conditions Aortopathy Panel, Sequencing and Deletion/Duplication Cardiology and Pulmonology APC- and MUTYH-Associated Polyposis Panel, Sequencing and Deletion/Duplication Gastroenterology Oncology 1 2 3 4 5 6 7 8 9 … Next › Last » 1 2 A B C D E F G H I J K L M N O P R S T U V W X Y
1p/19q Deletion in Oligodendrogliomas
21-Hydroxylase Deficiency Congenital Adrenal Hyperplasia – 21-OHD CAH
Acute Lymphoblastic Leukemia – ALL
Acute Lymphoblastic Leukemia FISH Panels
Acute Myeloid Leukemia – AML
Acute Myeloid Leukemia Mutation Panel by Next Generation Sequencing
Alloimmune Hemolytic Disease of the Fetus and Newborn (RhCc, RhEe, RhD, or Kell Antigen Genotyping)
Alpha Thalassemia
Alpha-1-Antitrypsin Deficiency Testing
Alpha-Iduronidase Enzyme Activity in Leukocytes
Alport Syndrome Panel, Sequencing and Deletion/Duplication
Alzheimer’s Disease
Amenorrhea
Amenorrhea Testing Algorithm
Angelman Syndrome and Prader-Willi Syndrome
Angelman Syndrome and Prader-Willi Syndrome by Methylation-Specific MLPA
Ankylosing Spondylitis (HLA-B27) Genotyping
Aortopathy Panel, Sequencing and Deletion/Duplication
APC- and MUTYH-Associated Polyposis Panel, Sequencing and Deletion/Duplication