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Searched: Congenital Hereditary Endothelial Dystrophy Type 2 (CHED2) and Harboyan Syndrome via SLC4A11 Gene Sequencing with CNV Detection
Search Results
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Test CodeMethodPrice7829Sequencing with CNV PG-Select$990
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Test CodeMethodPrice2720Sanger Sequencing$7808387Sequencing with CNV PGxome$990
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Test CodeMethodPrice3029Sequencing with CNV PGxome$990
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Test CodeMethodPrice2723Sanger Sequencing$110012015Sequencing with CNV PGxome$990
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Test CodeMethodPrice11171Sequencing with CNV PGxome$990912Sanger Sequencing$710
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Test CodeMethodPrice11065Sequencing with CNV PGxome$990862Sanger Sequencing$770
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Test CodeMethodPrice12003Sequencing with CNV PGxome$1290
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Test CodeMethodPrice3059Sequencing with CNV PG-Select$990
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Test CodeMethodPrice1478Sanger Sequencing$44010045Sequencing with CNV PGxome$990
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Test CodeMethodPrice12005Sequencing with CNV PGxome$1790
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Test CodeMethodPrice15223Sequencing with CNV PG-Select$990
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Test CodeMethodPrice1266Sanger Sequencing$6108723Sequencing with CNV PGxome$990
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Test CodeMethodPrice1547Sanger Sequencing$7808391Sequencing with CNV PGxome$990
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Test CodeMethodPrice2781Sanger Sequencing$9108197Sequencing with CNV PGxome$990
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Test CodeMethodPrice11075Sequencing with CNV PGxome$990698Sanger Sequencing$4070
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Test CodeMethodPrice2508Sanger Sequencing$6808561Sequencing with CNV PGxome$990
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Test CodeMethodPrice213Sanger Sequencing$5408987Sequencing with CNV PGxome$990
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Test CodeMethodPrice10335Sequencing with CNV PGxome$990
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