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- Steroid Genetics
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- Thyroglobulin
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- Thyrotrophin Binding Inhibiting Immunoglobulin
- Total Immunoreactive Calcitonin
- Vasoactive Intestinal Peptide
- α-Fetoprotein
- Metabolism
- Genetic Enzymes
- 3-Methylcrotonyl-CoA Carboxylase
- 3-Methylcrotonylglycinuria
- a-Fucosidase
- a-Galactosidase A
- a-Galactosidase A
- a-Glucosidase
- a-Idurodinase
- a-Ketoacid Decarboxylase
- a-Mannosidase
- a-Mannosidosis
- a-N-Acetylgalactosaminidase
- a-N-Acetylneuraminidase
- Acid Esterase
- Adrenomyeloneuropathy
- Amino Acid And Organic Acid Disorders
- Argininosuccinic Aciduria
- Arylsulphatase A
- Arylsulphatase B
- Arylsulphatase C
- Aspartylglucosaminidase
- Aspartylglycosaminuria
- b-Galactosidase
- b-Glucosidase
- b-Glucuronidase
- b-Hexosaminidase
- b-Mannosidase
- b-Mannosidosis
- Carbamoyl Phosphate Synthetase
- Carbamoyl Phosphate Synthetase Deficiency
- Catalase Latency
- Ceramidase
- Chitotriosidase
- Cholesterol Ester Storage Disease
- Cholesterol Esterification
- Cholesterol Storage
- Citrullinaemia
- Classical Galactosaemia
- Cystinosis
- Dihydroxyacetone Phosphate Acyl Transferase (DHAP-AT)
- Disorder of Branched-Chain Amino Acid Metabolism
- Disorders Of Galactose Metabolism
- Disorders of Organic Acid Metabolism
- Disorders of Sulphur Amino Acid Metabolism
- Fabry Disease
- Farber Disease
- Fucosidosis
- Galactocerebrosidase
- Galactokinase
- Galactokinase Deficiency Galactosaemia
- Galactose 1-Phosphate Uridyl Transferase
- Galactose 6-Sulphatase
- Galactosialidosis
- Gaucher Disease
- Generalised Peroxisomal Disorders
- Glucosamine N-Acetyltransferase
- Glycogen Storage Disease
- Glycosaminoglycans
- GM1-Gangliosidosis
- Heparan Sulphamidase
- Hunter Disease
- Hurler Disease and Scheie Disease
- I-Cell Disease and Pseudo-Hurler Polydystrophy
- Iduronate Sulphatase
- Infantile N-Acetylneuraminic Acid Storage Disease
- Krabbe Disease
- Lysosomal Enzyme Processing Defects
- Lysosomal Enzyme Screening
- Lysosomal Storage Disorders
- Maple Syrup Urine Disease
- Maroteaux-Lamy Disease
- Metachromatic Leucodystrophy
- Miscellaneous Disorders
- Morquio Disease
- Mucolipidoses
- Mucopolysaccharidoses (MPS)
- Mucopolysaccharidosis Type I
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- Mucopolysaccharidosis Type III
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- Mucopolysaccharidosis Type VI
- Mucopolysaccharidosis Type VII
- Mucosulphatidosis
- Multiple Carboxylase Deficiency
- Multiple Sulphatase Deficiency
- N-Acetylgalactosamine 6-Sulphatase
- N-Acetylneuraminic Acid
- Niemann-Pick Disease Type C
- Niemann-Pick Disease Types A and B
- Oligosaccharides
- Ornithine Transcarbamylase
- Ornithine Transcarbamylase Deficiency
- Other Lysosomal Disorders
- Peroxisomal Disorders
- Plasmalogen Biosynthesis
- Pompe Disease
- Pompe Disease and Glycogen Storage Disease Type II
- Propionic Acidaemia
- Propionyl-CoA Carboxylase
- Pseudo-Hurler Polydystrophy
- Pyruvate Carboxylase Deficiency
- Rhizomelic Chondrodysplasia Punctata
- Salla Disease
- Sandhoff Disease
- Sanfilippo Disease
- Scheie Disease
- Schindler Disease
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- Transport Defects
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- Very Long Chain Fatty Acids
- Wolman Disease
- X-Linked Adrenoleucodystrophy
- [14C]-Citrulline Incorporation
- [35S]-Cystine Incorporation
- Neurometabolism
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- Protein Reference Units
- a1 Antichymotrypsin
- a1 Antitrypsin Phenotyping
- Acetylcholine Receptor Antibody
- Acetylcholinesterase Isoenzyme (Amniotic Fluid)
- Adverse (Anaphylactoid) Reactions to Intravenous Drugs
- b2 Microglobulin
- Bence Jones Protein – in oncology only
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- Ceruloplasmin
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- Complement CH50
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Centres for Analysis and Clinical Interpretation