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Products found: 10Search results

Monash Medical Centre, Genetics and Molecular Pathology

Disorder Genes Test Method Lab Info Product code  
Monash Medical Centre, Genetics and Molecular Pathology Beckwith-Wiedemann Syndrome Methylation analysis
Monash Medical Centre, Genetics and Molecular Pathology Beckwith-Wiedemann Syndrome Sequence analysis of the entire coding region
Monash Medical Centre, Genetics and Molecular Pathology Beckwith-Wiedemann Syndrome Uniparental disomy study (UPD)
Monash Medical Centre, Genetics and Molecular Pathology Chromosome 11p15.5-Related Russell-Silver Syndrome H19, IGF2, Methylation analysis
Monash Medical Centre, Genetics and Molecular Pathology Rhabdoid Tumor Predisposition Syndrome 1 SMARCB1, Deletion/duplication analysis
Monash Medical Centre, Genetics and Molecular Pathology Rhabdoid Tumor Predisposition Syndrome 1 SMARCB1, Mutation scanning of the entire coding region
Monash Medical Centre, Genetics and Molecular Pathology Wilms Tumor-Aniridia-Genital Anomalies-Retardation Syndrome WT1, Deletion/duplication analysis
Monash Medical Centre, Genetics and Molecular Pathology WT1-Related Disorders WT1, Deletion/duplication analysis
Monash Medical Centre, Genetics and Molecular Pathology WT1-Related Disorders WT1, Mutation scanning of select exons
Monash Medical Centre, Genetics and Molecular Pathology WT1-Related Disorders WT1, Sequence analysis of select exons
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