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مختبرات الحياة الطبية - جده
Showing 421 to 441 of 637 entries
فحص
Cystic fibrosis Middle East Panel of common (CFTR)Cystic fibrosis Middle East Panel of common (CFTR)
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Fanconi anemia Panel (BRCA2, BRIP1, FANCA, FANCB,q
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frontometaphyseal dysplasia (FLNA) Sequencing
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Fructose-1,6-bisphosphatase deficiency (FBP1) Sequ
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Fructose-1,6-bisphosphatase deficiency (FBP1) Dele
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Galactosemia (GALT) Sequencing
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Gaucher disease (GBA) Sequencing
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Glycogen storage diseases Basic Panel (G6PC, SLC37
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Deafness, non-syndromic sensorineural autosomal re
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Deafness, non-syndromic sensorineural autosomal do
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Joubert syndrome gene Panel (26 genese) sequencing
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Joubert syndrome gene Panel (26 genese) by Deletio
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Mitochondrial diseases gene Panel (22 genesf) sequ
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Mitochondrial diseases gene Panel (22 genesf) by D
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Hypoparthyroidism-retardation-dysmorphism (Sanjad-
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AIRE gene (Autoimmune polyendocrinopathy syndrome
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Neutropenia, severe congenital type 1 or cyclic ne
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Ceroid Lipofuscinosis neuronal type 5 CLN5 gene si
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Pyruvate carboxylase deficiency (PC) gene sequenci
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Kallmann Syndrome KAL1 gene sequencing
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Limb Girdle Muscular Dystrophy gene panel deletion
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