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مختبرات الحياة الطبية - ينبع
Showing 253 to 273 of 645 entries
فحص
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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فحص
Joubert syndrome gene Panel (26 genese) sequencing
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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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Hypoparthyroidism-retardation-dysmorphism (Sanjad-
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فحص
AIRE gene (Autoimmune polyendocrinopathy syndrome
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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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Limb Girdle Muscular Dystrophy gene panel deletion
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فحص
Limb Girdle Muscular Dystrophy gene panel sequenci
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فحص
SCN1A gene sequencing for SCN1A-related seizure di
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Treacher Collins syndrome type 1, TCOF1 gene seque
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فحص
Treacher Collins syndrome type 1, TCOF1 gene delet
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فحص
Duchenne/ Becker Muscle Dystrophy (DMD/BMD) Diagno
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فحص
Spinal Muscular Atrophy (SMA) Diagnostic Test (SMN
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