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مختبرات الحياة الطبية - جده
Showing 400 to 420 of 637 entries
فحص
Ichthyosis, lamellar type 1 gene TGM1 full gene se
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Primary Dystonia Evaluation: TOR1A (DYT1) gene and
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Achondroplasia (FGFR3) Sequencing
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Alstrom syndrome (ALMS1) Sequencing
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Arginase deficiency (ARG1) Sequencing
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Von wille brand Factor activity (Ristocetin Cofactor)
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Glutamate Decarboxylase Abs in serum (Anti GAD)
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Tacrolimus (FK506)
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Erythropoietin (EPO)
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CA 50
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Dopamine Beta Hydroxylase
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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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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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فحص
Multiple joint dislocations, short stature, cranio
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فحص
Craniofacial and neuro-developmental abnormalities
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