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مختبرات الحياة الطبية - جده
Showing 379 to 399 of 652 entries
فحص
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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Special Stain
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Research
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Paraffin section for NSE
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Paraffin section for HER-2 neu
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Paraffin section for CD4
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