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Products found: 92Search results

Alberta Children's Hospital, Molecular Diagnostic Laboratory

Disorder Genes Test Method Lab Info Product code  
Alberta Children's Hospital, Molecular Diagnostic Laboratory 21-Hydroxylase-Deficient Congenital Adrenal Hyperplasia CYP21A2, Deletion/duplication analysis
Alberta Children's Hospital, Molecular Diagnostic Laboratory 21-Hydroxylase-Deficient Congenital Adrenal Hyperplasia CYP21A2, Sequence analysis of the entire coding region
Alberta Children's Hospital, Molecular Diagnostic Laboratory 21-Hydroxylase-Deficient Congenital Adrenal Hyperplasia CYP21A2, Targeted mutation analysis
Alberta Children's Hospital, Molecular Diagnostic Laboratory 3-Methylglutaconic Aciduria Type 5 DNAJC19, Sequence analysis of the entire coding region
Alberta Children's Hospital, Molecular Diagnostic Laboratory Achondroplasia FGFR3, Sequence analysis of select exons
Alberta Children's Hospital, Molecular Diagnostic Laboratory Achondroplasia FGFR3, Targeted mutation analysis
Alberta Children's Hospital, Molecular Diagnostic Laboratory Alpha-Thalassemia HBA1, HBA2, HBZ, Deletion/duplication analysis
Alberta Children's Hospital, Molecular Diagnostic Laboratory Alpha-Thalassemia HBA1, HBA2, HBZ, Sequence analysis of the entire coding region
Alberta Children's Hospital, Molecular Diagnostic Laboratory Alpha-Thalassemia HBA1, HBA2, HBZ, Targeted mutation analysis
Alberta Children's Hospital, Molecular Diagnostic Laboratory Angelman Syndrome UBE3A, Deletion/duplication analysis
Alberta Children's Hospital, Molecular Diagnostic Laboratory Angelman Syndrome UBE3A, Methylation analysis
Alberta Children's Hospital, Molecular Diagnostic Laboratory Angelman Syndrome UBE3A, Uniparental disomy study (UPD)
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