Genetic Diagnosis

Neuromuscular Disorders

 

-Duchenne Muscular Dystrophy Gene Deletions

-Duchenne Muscular Dystrophy MLPA Analysis

-Becker Muscular Dystrophy Gene Deletions

-Spinal Muscular Atrophy Gene Deletions

-Huntington Disease Genetic Analyses (trinucleotide repeat expansion analysis)

 

Hematological Malignancies

 

-ALL t(9;22) BCR- Abl p190,

-ALL t(9;22) BCR- Abl p210,

-ALL t(4;11)

-ALL t(12;21)

-ALL t(1;19)

-AML t(15;17)

-AML t(8;21)

-AML İnv(16)

-KML t(9;22) Quantitative -ABL Tyrosine Kinase Gene Mutations

-FLT3-ITD and D385 Gene Mutations

 

Coagulation Diagnosis

-Factor V (Leiden) Mutation

-Prothrombin G2021OA polymorphism

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