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مختبرات الحياة الطبية - جده
Showing 463 to 483 of 652 entries
فحص
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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Limb Girdle Muscular Dystrophy gene panel sequenci
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SCN1A gene sequencing for SCN1A-related seizure di
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Treacher Collins syndrome type 1, TCOF1 gene seque
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Treacher Collins syndrome type 1, TCOF1 gene delet
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Duchenne/ Becker Muscle Dystrophy (DMD/BMD) Diagno
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Spinal Muscular Atrophy (SMA) Diagnostic Test (SMN
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Adrenoleukodystrophy, X-linked ABCD1 gene sequenci
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Spinocerebellar Ataxia Type 7 (AD) ATXN7 gene repe
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Glycogen Storage Disease Type VI
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PHOX2B gene sequence analysis for congenital centr
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PHOX2B gene screening for congenital central hypov
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فحص
Glycogen Storage Disease Type VI (Sing Mutation)
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