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

✍ Scribed by Hallam, Stephanie; Faulkner, Nicole; Neitzel, Dana; Rochelle, Robert; Greger, Valerie

• Book ID: 122281321
• Publisher: Elsevier Science
• Year: 2014
• Tongue: English
• Weight: 28 KB
• Volume: 101
• Category: Article
• ISSN: 1556-5653
• DOI: 10.1016/j.fertnstert.2013.11.057