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مختبرات بوابتك الطبية - النعيم
Showing 316 to 336 of 597 entries
فحص
Transferrin Saturation Ratio
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Congenital Adrenal hyperplasia (CYP21A2 21-hydroxy
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Anti Myeloperoxidase Abs (MPO)
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Cornelia-De-Lange syndrome Panel (HDAC8, NIPBL, RA
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Multiple joint dislocations, short stature, cranio
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Craniofacial and neuro-developmental abnormalities
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Fanconi anemia Panel (BRCA2, BRIP1, FANCA, FANCB,q
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frontometaphyseal dysplasia (FLNA) Sequencing
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Fructose-1,6-bisphosphatase deficiency (FBP1) Sequ
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Fructose-1,6-bisphosphatase deficiency (FBP1) Dele
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Galactosemia (GALT) Sequencing
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Gaucher disease (GBA) Sequencing
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Glycogen storage diseases Basic Panel (G6PC, SLC37
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Deafness, non-syndromic sensorineural autosomal re
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Deafness, non-syndromic sensorineural autosomal do
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Joubert syndrome gene Panel (26 genese) sequencing
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Joubert syndrome gene Panel (26 genese) by Deletio
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Mitochondrial diseases gene Panel (22 genesf) sequ
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Mitochondrial diseases gene Panel (22 genesf) by D
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Hypoparthyroidism-retardation-dysmorphism (Sanjad-
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AIRE gene (Autoimmune polyendocrinopathy syndrome
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