Provider Name
Service provider

Al Hayat Medical Laboratories - Jeddah

Showing 295 to 315 of 658 entries
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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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Glycogen Storage Disease Type VI (Sing Mutation)

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Haemoglobin Differentiation by(HPLC)

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Growth Hormone ( After Exercise)

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Brain Natriuretic Peptide(BNP)

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Aldosterone / Direct Renin Ratio

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