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Genetic Disorders
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Genetic Disorders
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“SPINAL MUSCULAR ATROPHY (SMA), CARRIER DETECTION” has been added to your cart.
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Genetic Disorders
NX GEN SEQ, MEGALOENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS
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Genetic Disorders
NX GEN SEQ, MICROPHTHALMIA/ANOPHTHALMIA/COLOBOMA SPECTRUM
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Genetic Disorders
NX GEN SEQ, OPHTHALMOPLEGIA
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Genetic Disorders
NX GEN SEQ, OPTIC ATROPHY
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Genetic Disorders
NX GEN SEQ, RETINITIS PIGMENTOSA
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Genetic Disorders
NX GEN SEQ, USHER SYNDROME
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Genetic Disorders
NX GEN WHOLE EXOME SEQUENCING
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Genetic Disorders
NX GEN WHOLE EXOME SEQUENCING, TRIO WHOLE EXOME SEQUENCING OF PROBAND & BOTH PARENTS
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Genetic Disorders
PRADER-WILLI SYNDROME MUTATION DETECTION, METHYLATION SPECIFIC PCR
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Genetic Disorders
RETT SYNDROME DETECTION
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Genetic Disorders
SANGER SEQUENCING, SINGLE VARIANT
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Genetic Disorders
SPINAL MUSCULAR ATROPHY (SMA), CARRIER DETECTION
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