✦ LIBER ✦

Carrier Screening of 4,200 IVF Patients Utilizing Next Generation DNA Sequencing Detects Common, Rare, and Otherwise Undetectable Mutations across Several Diseases

✍ Scribed by Greger, Valerie; Breton, Benjamin; Faulkner, Nicole; Kennedy, Caleb; Neitzel, Dana; Nizzari, Marcia; Porreca, Greg; Saunders, Patrick; Umbarger, Mark; Rochelle, Robert; Hallam, Stephanie

Book ID: 122102181
Publisher: Elsevier Science
Year: 2013
Tongue: English
Weight: 130 KB
Volume: 99
Category: Article
ISSN: 1556-5653
DOI: 10.1016/j.fertnstert.2013.01.078

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Carrier screening of 8,500 IVF patients

Carrier screening of 8,500 IVF patients utilizing next generation DNA sequencing detects common, rare and otherwise undetectable mutations across society-recommended diseases

✍ Hallam, S.; Faulkner, N.; Neitzel, D.; Chennagiri, N.; Rochelle, R.; Greger, V. 📂 Article 📅 2013 🏛 Elsevier Science 🌐 English ⚖ 73 KB

Carrier Screening of 16,500 Patients in

Carrier Screening of 16,500 Patients in the IVF Setting Utilizing Next Generation DNA Sequencing Detects Common, Rare and Otherwise Undetectable Mutations in Prevalent, Society-Recommended Diseases

✍ Hallam, Stephanie; Faulkner, Nicole; Neitzel, Dana; Rochelle, Robert; Greger, Va 📂 Article 📅 2014 🏛 Elsevier Science 🌐 English ⚖ 28 KB