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Searched: Skeletal Disorders and Joint Problems Sequencing Panel with CNV Detection
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Test CodeMethodPrice10631Sequencing with CNV PGxome$1790
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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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… • Spondyloepimetaphyseal Dysplasia • Spondyloepimetaphyseal Dysplasia • Stickler syndrome • TP63-related conditions • Treacher Collins Syndrome • Van Der Woude Syndrome Since the Skeletal Disorders and Joint Problems panel is based on whole exome sequencing…
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…Rickets Rubinstein-Taybi Syndrome Short stature Homeobox (SHOX)-related Haploinsufficiency Disorder Shwachman-Diamond Syndrome Skeletal Disorders and Joint Problems Skeletal Dysplasia Spondylocostal Dysostosis Stickler Syndrome Syndactyly Tooth Agenesis Townes-Brocks Syndrome Treacher Collins Syndrome Tricho-rhino-phalangeal Syndrome Van der Woude Syndrome…
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…Neutropenia Popliteal Pterygium Syndrome Porphyria Pseudoxanthoma Elasticum Skeletal Disorders and Joint Problems Tuberous Sclerosis Xeroderma Pigmentosum…
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…Rubinstein-Taybi Syndrome Skeletal Disorders and Joint Problems Skeletal Dysplasia Smith-Lemli-Opitz Syndrome Sterol Disorders Stickler Syndrome Strabismus Syndrome Syndactyly Townes-Brocks Syndrome Treacher Collins Syndrome Tricho-rhino-phalangeal Syndrome VACTERL Association Disorders Van der Woude Syndrome…
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… Neonatal Crisis Panel Comprehensive Epilepsy and Seizure Panel Comprehensive Inherited Metabolic Disorders and Mitochondrial Disorders Panel Comprehensive Movement Disorder Panel Skeletal Disorders and Joint Problems Panel Primary…
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Test CodeMethodPrice1620Sanger Sequencing$4409219Sequencing with CNV PGxome$990
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Test CodeMethodPrice13325Sequencing with CNV PGxome$990
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…PGmax™ - Comprehensive Inherited Metabolic Disorders and Mitochondrial Disorders Panel PGmax™ - Comprehensive Movement Disorder Panel PGmax™ - Skeletal Disorders and Joint Problems Panel PGmax™ - Primary Immunodeficiency and Lymphoid…
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Test CodeMethodPrice10347Sequencing with CNV PGxome$990
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Test CodeMethodPrice1792Sanger Sequencing$7508417Sequencing with CNV PGxome$990
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Test CodeMethodPrice7947Sequencing with CNV PGxome$1290
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Test CodeMethodPrice7913Sequencing with CNV PG-Select$990
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…Predisposition Panel Test Code Method Price 19998 Sequencing with CNV PGxome $1790 PGmaxTM - Skeletal Disorders and Joint Problems Panel Test Code Method Price 10631 Sequencing with CNV PGxome $1790 Paget Disease of Bone (PDB) Panel Test Code…
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…Predisposition Panel Test Code Method Price 19998 Sequencing with CNV PGxome $1790 PGmaxTM - Skeletal Disorders and Joint Problems Panel Test Code Method Price 10631 Sequencing with CNV PGxome $1790 Paget Disease of Bone (PDB) Panel Test Code…
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Test CodeMethodPrice13367Sequencing with CNV PGxome$99011945Sanger Sequencing$540
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Test CodeMethodPrice13369Sequencing with CNV PGxome$990
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Test CodeMethodPrice2338Sanger Sequencing$7509945Sequencing with CNV PGxome$990
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Test CodeMethodPrice10289Sequencing with CNV PGxome$990
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