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Searched: Ectodermal Dysplasia Sequencing Panel with CNV Detection
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…variants (CNVs). This panel will detect all these variant types. Notably, the vast majority of CNVs, including 16p11.2 deletion syndrome and Smith-Magenis syndrome (17p11.2) will be detected. This panel is not designed to diagnose Prader…
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Test CodeMethodPrice10223Sequencing with CNV PGxome$990
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Test CodeMethodPrice3383Sanger Sequencing$7508421Sequencing with CNV PGxome$990
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Test CodeMethodPrice11439Sequencing with CNV PGxome$990985Sanger Sequencing$780
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Test CodeMethodPrice8861Sequencing with CNV PGxome$9902293Sanger Sequencing$580
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Test CodeMethodPrice618Sanger Sequencing$6508647Sequencing with CNV PGxome$990
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Test CodeMethodPrice7631Sequencing with CNV PG-Select$990
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Test CodeMethodPrice7033Sequencing with CNV PG-Select$990
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Test CodeMethodPrice2732Sanger Sequencing$5808863Sequencing with CNV PGxome$990
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Test CodeMethodPrice968Sanger Sequencing$8408285Sequencing with CNV PGxome$990
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Test CodeMethodPrice11367Sequencing with CNV PGxome$990
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Test CodeMethodPrice3021Sequencing with CNV PGxome$990
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…Myopathy, Areflexia, Respiratory Distress, and Dysphagia (EMARDD) via the MEGF10 Gene Test Code Method Price 11467 Sequencing with CNV PGxome $990 922 Sanger Sequencing $1210 Ectodermal Dysplasia Panel Test Code Method Price 10223…
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…, and Dysphagia (EMARDD) via the MEGF10 Gene Test Code Method Price 11467 Sequencing with CNV PGxome $990 922 Sanger Sequencing $1210 Ectodermal Dysplasia Panel Test Code Method Price 10223 Sequencing with CNV PGxome $990 Ectodermal Dysplasia…
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Test CodeMethodPrice8263Sequencing with CNV PGxome$990834Sanger Sequencing$870
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Test CodeMethodPrice12683Sequencing with CNV PGxome$1290
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Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia and DSP-Related Disorders via the DSP Gene
Test CodeMethodPrice11267Sequencing with CNV PGxome$990203Sanger Sequencing$1690 -
Test CodeMethodPrice619Sanger Sequencing$6108803Sequencing with CNV PGxome$990
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…Congenita Ectodermal Dysplasia Epiphyseal Dysplasia Facial Dysostosis Related Disorders Floating-Harbor Syndrome Gorlin Syndrome Greig Cephalopolysyndactyly Syndrome Holt-Oram Syndrome (HOS) Hypophosphatasia (HPP) Kenny-Caffey Syndrome…
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…Tract (CAKUT) Congenital Disorders of Glycosylation Congenital Limb Malformation Cornelia de Lange Syndrome Craniosynostosis Ectodermal Dysplasia Fetal Akinesia Deformation Sequence (FADS)/Le Fibrosis of Extraocular Muscles Floating-Harbor…
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