Provider Name
مزود الخدمة

مختبرات الحياة الطبية - ينبع

Showing 211 to 231 of 656 entries
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Primary Dystonia Evaluation: TOR1A (DYT1) gene and

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Prenatal diagnosis of a single gene disorder with

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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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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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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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