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…et al. 2017. PubMed ID: 28079900). Background Many known monogenic diseases present early in life as severe neonatal or early childhood (less than 2 years old) illness. In the United States, such diseases account for ~20% of infant deaths…
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…, neurological disease caused by the degeneration of motor neurons. Major clinical features are muscle weakness, atrophy, and eventually paralysis (Hardiman et al. 2017). The annual incidence of ALS is 2-3 per 100,000. Disease progression is rapid…
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…have shown genetic testing in such patients often yields a molecular diagnosis that allows for early intervention for the patient, proper genetic counseling of the family, and shortened diagnostic odysseys (Ceyhan-Birsoy et al. 2017. PubMed ID…
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Test CodeMethodPrice10155Sequencing with CNV PGxome$990
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Test CodeMethodPrice12976Repeat-Primed PCR & Fragment Length$350
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…Blog Post Link to Article Women’s History Month Published on March 6, 2017 This March, in honor of Women’s History Month, PreventionGenetics would like to recognize some of the remarkable women who contributed to the field of genetics…
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…(Hardiman et al. 2017. PubMed ID: 28980624). The dysfunction and loss of these neurons results in rapid progressive muscle weakness, atrophy and ultimately paralysis of limb, bulbar and respiratory muscles. About 50% of patients also develop…
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…et al. 2017. PubMed ID: 28079900; Kingsmore. 2012. PubMed ID: 22872815; Meng et al. 2017. PubMed ID: 28973083; Saunders et al. 2012. PubMed ID: 23035047; Stark et al. 2017. PubMed ID: 28125081). In recent studies, thorough curation…
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Test CodeMethodPrice10463Sequencing with CNV PGxome$990
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Test CodeMethodPrice8835Sequencing with CNV PGxome$9902008Sanger Sequencing$580
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Test CodeMethodPrice11733Sequencing with CNV PGxome$9901421Sanger Sequencing$750
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Test CodeMethodPrice1917Sequencing with CNV PG-Select$990
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