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Searched: Fetal Concerns 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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…sequencing tests, including the Fetal and Neonatal Loss Panel. There will be no extra charge for CNV detection. CNV detection via exome sequencing is equally or more sensitive than CMA. This new option provides the opportunity to bypass…
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…disorders, glycogen storage disorders, Noonan syndrome, and sudden cardiac death disorders (Wapner 2010; McPherson and Cold 2016; Sahoo et al. 2016). Our Panel The Fetal Concerns Panel includes sequencing and copy number variation detection of 40…
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…disorders. PreventionGenetics' Fetal Concerns Panel includes sequencing and copy number variation (CNV) detction for 40 genes.The 40 gene panel of single gene disorders was developed under collaboration between dual-certified molecular…
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…Metabolism of Cobalamin, Folate and Homocysteine Microcephaly Microphthalmia Myofibromatosis Neonatal and Fetal Concerns Nevoid Basal Cell Carcinoma Syndrome Opitz G Overgrowth Syndrome Polydactyly Premature Ovarian Failure (POF1) Rasopathies…
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…, and Lipoprotein Hypoglycemia Leber Hereditary Optic Neuropath Lysosomal Disorders Metabolic Myopathies, Rhabdomyolysis and Exercise Intolerance Metal Metabolism or Transport Disorders Mitochondrial DNA Mitochondrial Disorders Neonatal and Fetal Concerns Organic Acidemia/Acidurias Peroxisomal Disorders Phenotype Based Panels - Metabolic & Mitochon Porphyria…
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…specimen type is dependent on the fetal testing requested. Direct CVS or amniotic fluid samples can be accepted only for targeted prenatal testing. Any of the aforementioned sample types are accepted for full gene sequencing. Retention…
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Test CodeMethodPrice13083Sequencing with CNV PGxome$990
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Test CodeMethodPrice1025Sanger Sequencing$131011031Sequencing with CNV PGxome$990
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Test CodeMethodPrice10291Sequencing with CNV PGxome$990
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…Dr. Diane Allingham-Hawkins, Ph.D, FCCMG, FACM, the Senior Laboratory Director & Dean of Geneticists at PreventionGenetics presents "Getting More From Your Sequencing Test Copy Number Variant Detection by Next Generation Sequencing…
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…Pulmonology Our high quality pulmonology genetic test menu offers panels for various respiratory disorders and has been designed by our expert PhD team. PreventionGenetics’ genetic test menu includes tests for various pulmonology concerns…
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Test CodeMethodPrice7389Sequencing with CNV PG-Select$990
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…test menu that offers genetic tests and panels for various vision concerns, including, but not limited to cataracts, glaucoma, cone-rod dystrophy and more. CMA Achromatopsia Albinism Alport Syndrome Anophthalmia Anterior Segment Dysgenesis…
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…, and genetic testing. Our expert PhD team has skillfully constructed our skeletal and dental genetic test menu to offer a wide range of panels for skeletal and/or dental concerns. CMA Achondroplasia Adams-Oliver Syndrome Agnathia-Otocephaly…
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Test CodeMethodPrice4649Sequencing with CNV PG-Select$990
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Test CodeMethodPrice7517Sequencing with CNV PG-Select$990
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…variant (CNV) or genome-wide structural variant (SV) - depending on which platform you choose. Why Choose Large Panel Tests? There are many scenarios where a single-gene or smaller panel tests may be appropriate for your patient, including…
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…lacked testing options. DNA banking allowed for individuals to securely store their DNA to be used when testing advanced. Today, genomic testing is available at PreventionGenetics, and we can reanalyze past sequencing results as our…
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Test CodeMethodPrice990Sanger Sequencing$990
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