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مختبرات الحياة الطبية - جده
Showing 421 to 441 of 652 entries
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TORCH IgM Profile
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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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Dystonia gene Panel Next generation gene sequencin
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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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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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