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

✍ Scribed by Hallam, S.; Faulkner, N.; Neitzel, D.; Chennagiri, N.; Rochelle, R.; Greger, V.

• Book ID: 123067877
• Publisher: Elsevier Science
• Year: 2013
• Tongue: English
• Weight: 73 KB
• Volume: 100
• Category: Article
• ISSN: 1556-5653
• DOI: 10.1016/j.fertnstert.2013.07.380