Last data update: Feb 24, 2021. (Total: 3532 publications since 2011)
|Query Trace: all>>W Harry Hannon[CDC Author]|
| Congenital adrenal hyperplasia cases identified by newborn screening in one- and two-screen states.
Patrice K Held, Stuart K Shapira, Cynthia F Hinton, Elizabeth Jones, W Harry Hannon, and Jelili Ojodu
Mol. Genet. Metab. 2015 Aug 12.
| Newborn blood spot screening test using multiplexed real-time PCR to simultaneously screen for spinal muscular atrophy and severe combined immunodeficiency.
Jennifer L Taylor, Francis K Lee, Golriz Khadem Yazdanpanah, John F Staropoli, Mei Liu, John P Carulli, Chao Sun, Steven F Dobrowolski, W Harry Hannon, and Robert F Vogt
Clin. Chem. 2015 Feb 61(2) 412-9
| Implementation of the first worldwide quality assurance program for cystic fibrosis multiple mutation detection in population-based screening.
Marie C Earley, Anita Laxova, Philip M Farrell, Rena Driscoll-Dunn, Suzanne Cordovado, Peter J Mogayzel, Michael W Konstan, and W Harry Hannon
Clin. Chim. Acta 2011 Jul 15. 412(15-16) 1376-81