research counsyl.com

Counsyl Research - Counsyl Research

Counsyl is dedicated to sharing data with the medical community through research and scientific collaboration. We have published our findings in several peer-reviewed scientific journals, including Genetics in Medicine, the American Journal of Medical Genetics, Genetic Testing and Molecular Biomarkers, and Fertility and Sterility. The authors from Counsyl have been .

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LINKS TO BUSINESS

Counsyl Genetic screening and support for women and their families

Introducing a fresh new look for counsyl. Detect more at-risk couples with expanded carrier screening. Provide reliable non-invasive prenatal screening results, the first time. Help your patients get ahead of hereditary cancer. Seamlessly integrate Counsyl screening with our supporting services. See how we are making genetic screening more accessible. Help your patients understand their screening results. Learn about inherited diseases you and your partner might carry.

Counsyl Clinical Impact of Expanded Carrier Screening

Landmark study demonstrates clinical impact of Expanded Carrier Screening. The largest, most diverse Expanded Carrier Screening study ever published shows that current guidelines can miss a significant percentage of affected pregnancies. An analysis of 94 severe and profound conditions. Chief Medical Officer, Counsyl.

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TITLE

Counsyl Research - Counsyl Research

DESCRIPTION

Counsyl is dedicated to sharing data with the medical community through research and scientific collaboration. We have published our findings in several peer-reviewed scientific journals, including Genetics in Medicine, the American Journal of Medical Genetics, Genetic Testing and Molecular Biomarkers, and Fertility and Sterility. The authors from Counsyl have been .

CONTENT

This domain research.counsyl.com has the following in the web page, "Vysotskaia VS, Hogan GJ, Gould GM, Wang X, Robertson AD, Haas KR, Theilmann MR, Spurka L, Grauman PV, Lai HH, Jeon D, Haliburton G, Leggett M, Chu CS, Iori K, Maguire JR, Ready K, Evans EA, Kang HP, Haque IS." Our analyzers observed that the website also stated " Development and validation of a 36-gene sequencing assay for hereditary cancer risk assessment." The Website also stated " Lazarin GA, Haque IS, Evans EA, Goldberg JD. Smith-Lemli-Opitz syndrome carrier frequency and estimates of in utero mortality rates. Kaseniit KE, Theilmann MR."

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