These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
7. Improvement in cystic fibrosis newborn screening program outcomes with genetic counseling via telemedicine. Stalker HJ; Jonasson AR; Hopfer SM; Collins MS Pediatr Pulmonol; 2023 Dec; 58(12):3478-3486. PubMed ID: 37712603 [TBL] [Abstract][Full Text] [Related]
8. Outcomes of a cystic fibrosis carrier testing clinic for couples. Christie LM; Ingrey AJ; Turner GM; Proos AL; Watts GE Med J Aust; 2009 Nov; 191(9):499-501. PubMed ID: 19883345 [TBL] [Abstract][Full Text] [Related]
9. Cystic fibrosis: molecular diagnosis, population screening, and public policy. Grody WW Arch Pathol Lab Med; 1999 Nov; 123(11):1041-6. PubMed ID: 10539904 [TBL] [Abstract][Full Text] [Related]
10. Diagnosing cystic fibrosis in newborn screening in Poland - 15 years of experience. Sands D; Zybert K; Mierzejewska E; OĊtarzewski M Dev Period Med; 2015; 19(1):16-24. PubMed ID: 26003066 [TBL] [Abstract][Full Text] [Related]
12. Molecular testing for cystic fibrosis carrier status practice guidelines: recommendations of the National Society of Genetic Counselors. Langfelder-Schwind E; Karczeski B; Strecker MN; Redman J; Sugarman EA; Zaleski C; Brown T; Keiles S; Powers A; Ghate S; Darrah R J Genet Couns; 2014 Feb; 23(1):5-15. PubMed ID: 24014130 [TBL] [Abstract][Full Text] [Related]
13. Carrier screening for cystic fibrosis: a perinatal perspective. Demsey SA J Perinat Neonatal Nurs; 1999 Sep; 13(2):14-26. PubMed ID: 10818851 [TBL] [Abstract][Full Text] [Related]
14. An update on cystic fibrosis screening. Goetzinger KR; Cahill AG Clin Lab Med; 2010 Sep; 30(3):533-43. PubMed ID: 20638569 [TBL] [Abstract][Full Text] [Related]
15. Genetic counseling and neonatal screening for cystic fibrosis: an assessment of the communication process. Ciske DJ; Haavisto A; Laxova A; Rock LZ; Farrell PM Pediatrics; 2001 Apr; 107(4):699-705. PubMed ID: 11335747 [TBL] [Abstract][Full Text] [Related]
16. The cystic fibrosis transmembrane conductance regulator gene and ion channel function in patients with idiopathic pancreatitis. Bishop MD; Freedman SD; Zielenski J; Ahmed N; Dupuis A; Martin S; Ellis L; Shea J; Hopper I; Corey M; Kortan P; Haber G; Ross C; Tzountzouris J; Steele L; Ray PN; Tsui LC; Durie PR Hum Genet; 2005 Dec; 118(3-4):372-81. PubMed ID: 16193325 [TBL] [Abstract][Full Text] [Related]
17. The c.1364C>A (p.A455E) Mutation in the CFTR Pseudogene Results in an Incorrectly Assigned Carrier Status by a Commonly Used Screening Platform. Deeb KK; Metcalf JD; Sesock KM; Shen J; Wensel CA; Rippel LI; Smith M; Chapman MS; Zhang S J Mol Diagn; 2015 Jul; 17(4):360-5. PubMed ID: 25956447 [TBL] [Abstract][Full Text] [Related]
18. Cystic fibrosis testing 8 years on: lessons learned from carrier screening and sequencing analysis. Strom CM; Crossley B; Buller-Buerkle A; Jarvis M; Quan F; Peng M; Muralidharan K; Pratt V; Redman JB; Sun W Genet Med; 2011 Feb; 13(2):166-72. PubMed ID: 21068670 [TBL] [Abstract][Full Text] [Related]
19. Genotyping microarray for the detection of more than 200 CFTR mutations in ethnically diverse populations. Schrijver I; Oitmaa E; Metspalu A; Gardner P J Mol Diagn; 2005 Aug; 7(3):375-87. PubMed ID: 16049310 [TBL] [Abstract][Full Text] [Related]
20. Screening practices for mutations in the CFTR gene ABCC7. Girodon-Boulandet E; Cazeneuve C; Goossens M Hum Mutat; 2000; 15(2):135-49. PubMed ID: 10649490 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]