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مختبرات الحياة الطبية - ينبع
Showing 148 to 168 of 616 entries
فحص
Vanil Mandelic Acid (VMA)
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C3 Complement
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Osteocalcin
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Haptoglobin
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Lactate in Plasma
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Metachromatic Leukodystrophy. ARSA gene single mut
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CADASIL (NOTCH3 Gene)
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Chromosome Analysis Amniotic Fluid
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Vitamin D 3 (1,25 Dihydroxycholecalciferol)
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Huntington Genetic Testing
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Cockayne Syndrome
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L-2-Hydroxyglutaric Aciduria (L2HG DH gene Sequenc
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Cornelia de Lange Syndrome gene Panel by NGS
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Congenital ichthyosis gene Panel (9 genes): includ
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Congenital Ichthyosis ABCA12 gene sequencing
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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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