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Products found: 13Search results

Centre for Cardiovascular Surgery and Transplantation, Molecular Genetics Laboratory

Disorder Genes Test Method Lab Info Product code  
Centre for Cardiovascular Surgery and Transplantation, Molecular Genetics Laboratory Autosomal Dominant Hyper IgE Syndrome STAT3, Sequence analysis of select exons
Centre for Cardiovascular Surgery and Transplantation, Molecular Genetics Laboratory Cardiovascular Disease Risk Factor (Apolipoprotein E) APOE, Targeted mutation analysis
Centre for Cardiovascular Surgery and Transplantation, Molecular Genetics Laboratory Complement Component C2 Deficiency C2, Targeted mutation analysis
Centre for Cardiovascular Surgery and Transplantation, Molecular Genetics Laboratory APOB-Related Familial Hypercholesterolemia, Autosomal Dominant APOB, Targeted mutation analysis
Centre for Cardiovascular Surgery and Transplantation, Molecular Genetics Laboratory Hereditary Angioedema SERPING1, Mutation scanning of the entire coding region
Centre for Cardiovascular Surgery and Transplantation, Molecular Genetics Laboratory Mannose-Binding Protein Deficiency MBL2, Targeted mutation analysis
Centre for Cardiovascular Surgery and Transplantation, Molecular Genetics Laboratory SH2D1A-Related Lymphoproliferative Disease, X-Linked SH2D1A, Sequence analysis of the entire coding region
Centre for Cardiovascular Surgery and Transplantation, Molecular Genetics Laboratory TNFRSF13B-Related Common Variable Immune Deficiency TNFRSF13B, Mutation scanning of select exons
Centre for Cardiovascular Surgery and Transplantation, Molecular Genetics Laboratory WAS-Related Disorders WAS, Sequence analysis of the entire coding region
Centre for Cardiovascular Surgery and Transplantation, Molecular Genetics Laboratory X-Linked Agammaglobulinemia BTK, Mutation scanning of the entire coding region
Centre for Cardiovascular Surgery and Transplantation, Molecular Genetics Laboratory X-Linked Hyper IgM Syndrome CD40LG, Sequence analysis of the entire coding region
Centre for Cardiovascular Surgery and Transplantation, Molecular Genetics Laboratory X-Linked Severe Combined Immunodeficiency IL2RG, Sequence analysis of the entire coding region
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