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PATHLABS
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Cardiology Test
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Whole Exome Sequencing+Mitochrondrial Disease Panel
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William’s Syndrome
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Willsons Disease Screening Panel: S. Copper, U. Copper, Ceruloplasmin)
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WT-1 Mutation Detection
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X & Y [Sex Mismatch Bone Marrow Transplant]
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X & Y Identification
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X & Y Identification
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XMN1 Polymorphism Testing
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Y Chromosome Microdeletion (16 Mutations)
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Y Chromosome Microdeletion (16 Mutations)
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Y Chromosome Microdeletion (16 Mutations)
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Zinc (Blood, Serum)
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