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Results: 3

1.

Genotypic diversity and mixed infection in newborn disease and hearing loss in congenital cytomegalovirus infection.

Pati SK, Pinninti S, Novak Z, Chowdhury N, Patro RK, Fowler K, Ross S, Boppana S; NIDCD CHIMES Study Investigators.

Pediatr Infect Dis J. 2013 Oct;32(10):1050-4. doi: 10.1097/INF.0b013e31829bb0b9.

2.

Saliva polymerase-chain-reaction assay for cytomegalovirus screening in newborns.

Boppana SB, Ross SA, Shimamura M, Palmer AL, Ahmed A, Michaels MG, Sánchez PJ, Bernstein DI, Tolan RW Jr, Novak Z, Chowdhury N, Britt WJ, Fowler KB; National Institute on Deafness and Other Communication Disorders CHIMES Study.

N Engl J Med. 2011 Jun 2;364(22):2111-8. doi: 10.1056/NEJMoa1006561.

3.

Dried blood spot real-time polymerase chain reaction assays to screen newborns for congenital cytomegalovirus infection.

Boppana SB, Ross SA, Novak Z, Shimamura M, Tolan RW Jr, Palmer AL, Ahmed A, Michaels MG, Sánchez PJ, Bernstein DI, Britt WJ, Fowler KB; National Institute on Deafness and Other Communication Disorders CMV and Hearing Multicenter Screening (CHIMES) Study.

JAMA. 2010 Apr 14;303(14):1375-82. doi: 10.1001/jama.2010.423.

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