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6. Population-based newborn screening for genetic disorders when multiple mutation DNA testing is incorporated: a cystic fibrosis newborn screening model demonstrating increased sensitivity but more carrier detections. Comeau AM, Parad RB, Dorkin HL, Dovey M, Gerstle R, Haver K, Lapey A, O'Sullivan BP, Waltz DA, Zwerdling RG, Eaton RB. Pediatrics; 2004 Jun; 113(6):1573-81. PubMed ID: 15173476 [Abstract] [Full Text] [Related]
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20. [Neonatal screening for cystic fibrosis]. Tellería Orriols JJ, Alonso Ramos MJ, Garrote Adrados JA, Fernández Carvajal I, Blanco Quirós A. An Esp Pediatr; 2002 Jul 03; 57(1):60-5. PubMed ID: 12139895 [Abstract] [Full Text] [Related] Page: [Next] [New Search]