Infant hearing loss and connexin testing in a diverse population

Genetics in Medicine - Tập 10 - Trang 517-524 - 2008
Lisa A. Schimmenti1, Ariadna Martinez2, Milhan Telatar3, Chih-Hung Lai3, Nina Shapiro4, Michelle Fox5, Berta Warman1, Matthew McCarra1, Barbara Crandall2,5, Yvonne Sininger4, Wayne W. Grody3,5,6, Christina G.S. Palmer2,6
1Department of Pediatrics, Institute of Human Genetics, University of Minnesota Medical School, Minneapolis, Minnesota;
2Departments of Psychiatry and Biobehavioral Sciences
3Departments of Pathology and Laboratory Medicine
4Departments of Surgery
5Departments of Pediatrics
6Departments of Human Genetics, The David Geffen School of Medicine at University of California, Los Angeles, Los Angeles, California.

Tài liệu tham khảo

Finitzo Fortnum Centers for Disease Control. Early Hearing Detection and Intervention (EHDI) Program. 2007. Available at: http://www.cdc.gov/NCBDDD/ehdi/default.htm. Accessed June 5, 2008. Yoshinaga-Itano Moeller Denoyelle Estivill Kelsell Prasad Rabionet Green Abe Morell Estivill X, Gasparini P. The Connexin-deafness homepage. Available at: http://davinci.crg.es/deafness Accessed June 4, 2008. Snoeckx Kenneson Pallares-Ruiz del Castillo American College of Medical Genetics Morton Schimmenti Kenneson Norris Pagarkar Ramsebner Cohn Joint Committee on Infant Hearing SAS Version 9, SAS Institute: Cary NC. Tang Pandya Cryns Huculak Dent Yaeger Putcha United State Census Bureau. American Community Survey 2005. Available at: http://factfinder.census.gov. Accessed August 5, 2007. Samanich Kimberling Ross Grody Norton Green
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Genetics in Medicine

Tập 10

517-524

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