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Searched: Alagille Syndrome 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 CodeMethodPrice10071Sequencing with CNV PGxome$990
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Test CodeMethodPrice15253Sequencing with CNV PG-Select$990
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Test CodeMethodPrice10229Sequencing with CNV PGxome$990
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Test CodeMethodPrice15259Sequencing with CNV PG-Select$990
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…features, clinical sensitivity and additional information. Noonan Spectrum Disorders/Rasopathies NextGen Sequencing Panel Alagille Syndrome NextGen Sequencing Panel Holt-Oram Syndrome (HOS) Testing via TBX5 Sequencing PreventionGenetics also…
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Test CodeMethodPrice10319Sequencing 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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Test CodeMethodPrice13041Sequencing with CNV PGxome$1190
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…of the genetic determinants of many gastrointestinal (GI) disorders. Genetic testing is an important step for gastroenterologists to consider for clinical care. CMA Alagille Syndrome Autoimmune Disease Autoimmune Lymphoproliferative Syndrome…
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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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…, the majority of causative variants are inherited (Francalanci et al. 2013. PubMed ID: 23437912). Alagille syndrome, an autosomal dominant disorder caused by defects in the JAG1 and NOTCH2 genes, is an example of hereditary cholestatic…
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…genetic testing is imperative for diagnostics and informed treatment decisions. CMA Aarskog-Scott Syndrome (Faciogenital Dysplasia) Achondroplasia Agnathia-Otocephaly Complex Alagille Syndrome Anophthalmia Arthrogryposis Axenfeld-Rieger…
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…., 2016). The genes associated with these syndromes are included in the Comprehensive Congenital Heart Disease panel, however, based on clinical features one of the smaller panels may be appropriate. Additional Testing Options Alagille…
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Test CodeMethodPrice13097Sequencing with CNV PGxome$990
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…, LAGE3, KAT2B, and LAMA5, and CNV detection. Kidney-Related Disorders Tests at PreventionGenetics PreventionGenetics also offers panels for many other kidney related disorders, including: Alport Syndrome (AS) Panel Alstrom Syndrome via…
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…Complex Panel Test Code Method Price 7955 Sequencing with CNV PGxome $990 Aicardi-Goutières Syndrome Panel Test Code Method Price 10237 Sequencing with CNV PGxome $990 Alagille Syndrome Panel Test Code Method Price 10071 Sequencing with CNV…
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…Test Code Method Price 10285 Sequencing with CNV PGxome $990 Primary Periodic Paralysis Panel Test Code Method Price 10139 Sequencing with CNV PGxome $990 Progressive Familial Intrahepatic Cholestasis (PFIC) and Alagille syndrome Panel…
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…Intrahepatic Cholestasis (PFIC) and Alagille syndrome Panel Test Code Method Price 10229 Sequencing with CNV PGxome $990 Prostate Cancer Panel Test Code Method Price 5459 Sequencing with CNV PG-Select $990 Pseudohypoaldosteronism Type I…
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Test CodeMethodPrice12003Sequencing with CNV PGxome$1290
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