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مختبرات الحياة الطبية - ينبع
Showing 232 to 252 of 629 entries
فحص
N-methyl-D-Aspatate Receptor (IgG)
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TB (AFB) Film
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Syphilis
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C6 Complement
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Bloom syndrome (BLM) Sequencing
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Transferrin Saturation Ratio
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Congenital Adrenal hyperplasia (CYP21A2 21-hydroxy
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فحص
Anti Myeloperoxidase Abs (MPO)
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فحص
Cornelia-De-Lange syndrome Panel (HDAC8, NIPBL, RA
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Multiple joint dislocations, short stature, cranio
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Cystic fibrosis Middle East Panel of common (CFTR)Cystic fibrosis Middle East Panel of common (CFTR)
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Lead in blood
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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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فحص
Deafness, non-syndromic sensorineural autosomal re
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فحص
Deafness, non-syndromic sensorineural autosomal do
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فحص
Joubert syndrome gene Panel (26 genese) sequencing
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