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ACHONDROPLASIA
ACUTE INTERMITTENT PORPHYRIA (AIP) - HMBS GENE - (B)
ALPHA THALASSEMIA - HBA1 GENE, HBA2 GENE - (B)
AMINOGLYCOSIDE OTOTOXICITY
AML/ETO - (BM)
AML/ETO - (B)
AML1/ETO - (BM)
AML1/ETO - (B)
ANGELMAN SYNDROME (AS) - (B)
APERT SYNDROME
APLASTIC ANEMIA COMPREHENSIVE ANALYSIS - (B)
APOLIPOPROTEIN E GENOTYPING (APOE) - (B)
ASHKENAZI JEWISH PANEL - HEXA, ASPA, IKBKAP, FANCC GENES - (B)
ATAXIA TELANGIECTASIA