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UCSDW3BG: Search by DNA test
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Enzyme Assay
Metabolite Assay
DNA Test
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21-Hydroxylase Mutation Analysis
Adenylosuccinate Lyase
Adrenocorticotropin (ACTH) Receptor Mutation Analysis
Alpha Thalassemia Mutation Analysis
Alpha-Glucosidase Mutations
Androgen Receptor (AR) Mutation Analysis
Androgen Receptor Triplet Expansion
Apolipoprotein E Genotype
Arginine Vasopressin (Neurophysin II) Genotyping
Arylsulfatase A Allele Analysis
Arylsulfatase A Mutations
Arylsulfatase A Pseudo-Deficiency
Ashkenazi Genetic Disease Screen
Aspartoacylase (Canavan) Mutation Analysis
ATP7A Mutation Analysis
Azoospermia DAZ/DAZLA mutation screen
Beta-Glucosidase Mutation Analysis
Bile Acid Transporter, Ileal, Mutation Analysis
Canavan Disease, DNA screen
Carbamyl Phosphate Synthase I Mutation Analy.
Carnitine Palmitoyltransferase II Mutation Analysis
Cerebrotendinous Xanthomatosis Mutation Analysis
CFTR Poly T Analysis
Charcot-Marie-Tooth CMT1A duplication
Chlamydia trichomatis
Connexin 26 Mutation Analysis
CPTII - Common Mutation Analysis
CPTII DNA Analysis - Panel of 9 mutations
Cystic Fibrosis Mutation Analysis
D15S63 Methylation
Dentatorubral-Pallidoluysian Atrophy Triplet Expansion
Dihydropyrimidine Dehydrogenase, Mutation Analysis
Dystrophin Multiplex PCR
Factor V Leiden
Factor V Leiden Mutation Screen
FMR-1 (Fragile X Syndrome) Triplet Repeat and Methylation
Frataxin Triplet Expansion
G-6-Pase Translocase Mutation Screen (GSD Ib DNA)
Galactose-1-P Uridyl Transferase Mutations
Glucose-6-Phosphatase DNA screen
Glutamate Dehydrogenase 1
Glycogen Debranching Enzyme Mutation Screen (GSD III-a/III-b DNA)
Gorlin (Nevoid Basal Cell Carcinoma) Syndrome, Mutation Anal
HCV quantification
Hemoglobin S,C DNA
Hemophilia A
Hexosaminidase A Mutational Analysis
HFE (Hereditary Hemochromatosis) Mutation Analysis
HIV Genotyping
HIV quantification
HLA typing
Huntington Disease Triplet Expansion
Hypoxanthine-Guanine Phosphoribosyl Transf.
Iduronidase Mutations
Long Chain Hydroxyacyl CoA Dehydrogenase Mutation Analysis
Long Chain Hydroxyacyl-CoA Dehydrogenase (LCHAD) DNA test
Long Chain Hydroxyacyl-CoA Dehydrogenase Genotyping
Machado-Joseph Disease (MJD-1) Triplet Expansion
Maternal Cell Contamination
MCAD - Unknown Mutation Detection by DNA Sequencing
MCAD DNA Analysis - Panel of 9 mutations
MCAD DNA screen
Medium Chain Acyl-CoA Dehydrogenase (MCAD) DNA test
Methylenetetrahydratefolate Reductase Genotyping
Methylenetetrahydratefolate Reductase, Mutation Analysis
Mitochondrial DNA Mutation Screen
Multiple Endocrine Neoplasia, Mutation Analysis
Myophosphorylase Mutation Screen
Myotonin Protein Kinase Triplet Repeat
Neisseria gonorrhoeae
Norrie gene
Ornithine Carbamoyltransferase Mutation Analysis
Ornithine Transcarbamylase Genotyping
Phenylalanine Hydroxylase (PKU) Mutations
Phosphofructokinase Mutation Analysis
Phosphoglycerate Mutase Mutation Analysis
Phosphorylase (GSD-V) Mutation Analysis
Pituitary Specific Transcription Factor-1 (POU1F1)
Polycystic Kidney Disease, Adult, Linkage
Prader-Willi/Angelman Methylation Studies
Procollagen type I (COL1A1, COL1A2) Mutation Analysis
Procollagen type II (COL2A1) Mutation Analysis
Prophet of Pit-1 (PROP-1) Mutation Analysis
Prothrombin Mutation Screen
Retinoblastoma gene
Short Chain Acyl-CoA Dehydrogenase (SCAD) Gene Variant DNA T
Short Chain Acyl-CoA Dehydrogenase Mutation Studies
Spinocerebellar Ataxia (SCA1) Genetics Test
Spinocerebellar Ataxia DNA Panel
SRY Mutation Screen
Sulfate Transporter DTDST Mutation Analysis
Survival Motor Neuron DNA Deletion Detection (Spinal Muscular Atrophy)
Twin Zygosity Studies
Uniparental Disomy DNA
Y Chromosome DNA
Y Chromosome Microdeletion Studies
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