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مختبرات الحياة الطبية - جده
Showing 442 to 462 of 598 entries
فحص
Craniofacial and neuro-developmental abnormalities
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فحص
Fanconi anemia Panel (BRCA2, BRIP1, FANCA, FANCB,q
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فحص
frontometaphyseal dysplasia (FLNA) Sequencing
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فحص
Fructose-1,6-bisphosphatase deficiency (FBP1) Sequ
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فحص
Fructose-1,6-bisphosphatase deficiency (FBP1) Dele
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فحص
Galactosemia (GALT) Sequencing
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فحص
Gaucher disease (GBA) Sequencing
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فحص
Glycogen storage diseases Basic Panel (G6PC, SLC37
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فحص
Deafness, non-syndromic sensorineural autosomal re
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فحص
Deafness, non-syndromic sensorineural autosomal do
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فحص
Joubert syndrome gene Panel (26 genese) sequencing
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فحص
Joubert syndrome gene Panel (26 genese) by Deletio
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فحص
Mitochondrial diseases gene Panel (22 genesf) sequ
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فحص
Mitochondrial diseases gene Panel (22 genesf) by D
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فحص
Hypoparthyroidism-retardation-dysmorphism (Sanjad-
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فحص
AIRE gene (Autoimmune polyendocrinopathy syndrome
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فحص
Neutropenia, severe congenital type 1 or cyclic ne
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فحص
Ceroid Lipofuscinosis neuronal type 5 CLN5 gene si
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فحص
Pyruvate carboxylase deficiency (PC) gene sequenci
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فحص
Kallmann Syndrome KAL1 gene sequencing
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فحص
Limb Girdle Muscular Dystrophy gene panel deletion
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