الفحوصات الجينية في مختبرات العولقي التخصصية
اضغط الرابط ادناة لتحميل ملف الفحوصات الجينية في مختبرات العولقي التخصصية :
https://aulaqilabs.com/upload/1685898049.pdf
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BCR -ABL Gene mutation
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BCR -ABL T3151 imatinib resistant
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PML RARA
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Congenital adrenal hyperplasia CAH
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FMF ( familial Mediterranean fever )
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Lactose Intolerance
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HLA AB DR
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HLA ABC DR DQ
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HLA B27
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HLA B50
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HLA B51
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Meningitis pathogens multiplex panel
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Respiratory pathogens multiplex panel
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Herpes simplex virus
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Human papilloma virus DNA genotyping HR
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Gaucher disease
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Cystic Fibrosis CFTR Gene Mutations (36 mutations), Blood
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cardio Vascular Disease Risk Factors, 12 Mutations Profile, PCR
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Factor II G20210A Prothrombin Gene Mutation (for CVD and Recurrent Abortion)
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Factor V G1691A (Leiden) Gene Mutation ( for CVD and Recurrent Abortion)
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Human Oncogenes, Breast Cancer genes (BRCA1, BRCA2) , Gene Analysis ,PCR
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JAK2 - gene - VAL617PHE (V617F) mutation - whole blood
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MTHFR C677T (for CVD and Recurrent Abortion)
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PCA3 - gene - prostate cancer marker - Messenger RNA detection
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Spinal Muscular Atrophy (SMA), Genetic Analysis
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Y Chromosome Microdeletions (6 deletions), PCR
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α-Globin Gene, α-Thalassemia, (21 mutations), PCR, Blood
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α-Globin Gene, α-Thalassemia, (21 mutations), PCR, Amniotic Fluid
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β-Globin Gene, β-Thalassemia, (22 mutations), PCR, Blood
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β-Globin Gene, β-Thalassemia, (22 mutations), PCR, Amniotic Fluid
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Human Papilloma Virus DNA Genotyping
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Hepatitis C Virus RNA, Quantitative
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Hepatitis C Virus RNA, Genotyping
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Hepatitis B Virus DNA, Quantitative
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TB PCR Qualitative
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CMV by PCR.
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EBV by PCR