Carrier Screening#17
Basic Carrier Screening Panel
Screens common carrier conditions before marriage or pregnancy.
العينةSampleBlood / Salivaالمدة المتوقعةTurnaround14 يومdays
Carrier Screening#4
Carrier Screening Panel
Screens carrier status for selected inherited disorders.
العينةSampleBlood / Salivaالمدة المتوقعةTurnaround14 يومdays
Carrier Screening#5
CFTR Cystic Fibrosis Mutation Test
Detects common CFTR gene variants associated with cystic fibrosis.
العينةSampleBlood / Buccal Swabالمدة المتوقعةTurnaround10 يومdays
Carrier Screening#23
Duchenne Muscular Dystrophy Carrier Test - DMD
Assesses DMD gene deletions/duplications or variants for carrier status.
العينةSampleBloodالمدة المتوقعةTurnaround21 يومdays
Carrier Screening#16
Expanded Carrier Screening Panel
Screens carrier status across a wide range of inherited recessive and X-linked disorders.
العينةSampleBlood / Salivaالمدة المتوقعةTurnaround21 يومdays
Carrier Screening#22
Familial Mediterranean Fever - MEFV Test
Detects selected MEFV variants related to familial Mediterranean fever.
العينةSampleBlood / Salivaالمدة المتوقعةTurnaround14 يومdays
Carrier Screening#18
Fragile X Premutation Carrier Test - FMR1
FMR1 CGG repeat analysis for carrier and premutation assessment.
العينةSampleBloodالمدة المتوقعةTurnaround14 يومdays
Carrier Screening#21
G6PD Gene Mutation Test
Detects selected G6PD variants associated with enzyme deficiency.
العينةSampleBlood / Buccal Swabالمدة المتوقعةTurnaround10 يومdays
Carrier Screening#24
Hemophilia A Carrier Test - F8
Genetic testing for carrier status in families with hemophilia A.
العينةSampleBloodالمدة المتوقعةTurnaround21 يومdays
Carrier Screening#25
Hemophilia B Carrier Test - F9
Genetic testing for carrier status in families with hemophilia B.
العينةSampleBloodالمدة المتوقعةTurnaround21 يومdays
Carrier Screening#6
SMA - SMN1 Copy Number Test
Assesses SMN1 copy number for spinal muscular atrophy carrier status.
العينةSampleBlood / Salivaالمدة المتوقعةTurnaround10 يومdays
Carrier Screening#19
Thalassemia Alpha Globin Gene Test - HBA1/HBA2
Detects common alpha globin deletions or variants.
العينةSampleBloodالمدة المتوقعةTurnaround14 يومdays
Carrier Screening#20
Thalassemia Beta Globin Gene Test - HBB
Detects common beta globin variants associated with beta thalassemia.
العينةSampleBloodالمدة المتوقعةTurnaround14 يومdays
Newborn Screening#48
Biotinidase Deficiency - BTD Test
Detects BTD variants associated with biotinidase deficiency.
العينةSampleBlood / Dried Blood Spotالمدة المتوقعةTurnaround14 يومdays
Newborn Screening#47
GALT Galactosemia Genetic Test
Detects selected GALT variants associated with galactosemia.
العينةSampleBlood / Dried Blood Spotالمدة المتوقعةTurnaround14 يومdays
Newborn Screening#45
Hearing Loss Newborn Genetic Panel
Detects common genetic causes of congenital or early-onset hearing loss.
العينةSampleBlood / Buccal Swabالمدة المتوقعةTurnaround21 يومdays
Newborn Screening#43
Newborn Genetic Screening Panel
Screens newborns for selected inherited metabolic and genetic disorders.
العينةSampleDried Blood Spot / Bloodالمدة المتوقعةTurnaround14 يومdays
Newborn Screening#44
Newborn Metabolic Disease Gene Panel
Gene panel for selected inherited metabolic diseases.
العينةSampleBlood / Dried Blood Spotالمدة المتوقعةTurnaround21 يومdays
Newborn Screening#46
SCID Newborn Genetic Test
Genetic assessment for selected severe combined immunodeficiency genes.
العينةSampleBlood / Dried Blood Spotالمدة المتوقعةTurnaround21 يومdays