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مختبرات الحياة الطبية - جده
Showing 421 to 441 of 598 entries
فحص
Congenital Ichthyosis ABCA12 gene sequencing
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فحص
Dystonia gene Panel Next generation gene sequencin
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فحص
Ichthyosis, lamellar type 1 gene TGM1 full gene se
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فحص
Primary Dystonia Evaluation: TOR1A (DYT1) gene and
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فحص
Achondroplasia (FGFR3) Sequencing
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Alstrom syndrome (ALMS1) Sequencing
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فحص
Arginase deficiency (ARG1) Sequencing
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فحص
Glutamate Decarboxylase Abs in serum (Anti GAD)
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فحص
Tacrolimus (FK506)
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فحص
Erythropoietin (EPO)
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فحص
CA 50
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Dopamine Beta Hydroxylase
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N-methyl-D-Aspatate Receptor (IgG)
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فحص
TB (AFB) Film
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فحص
Syphilis
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فحص
C6 Complement
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فحص
Transferrin Saturation Ratio
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فحص
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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فحص
Multiple joint dislocations, short stature, cranio
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