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7. Prenatal screening for cystic fibrosis: where are we now? Farrell PM; Fost N J Pediatr; 2002 Dec; 141(6):758-63. PubMed ID: 12461490 [No Abstract] [Full Text] [Related]
8. Prenatal diagnosis for cystic fibrosis using SSCP analysis. Desgeorges M; Boulot P; Kjellberg P; Lefort G; Rolland M; Demaille J; Claustres M Prenat Diagn; 1993 Feb; 13(2):147-8. PubMed ID: 7681978 [No Abstract] [Full Text] [Related]
9. Clinical experience with preimplantation genetic diagnosis of cystic fibrosis (delta F508). Ao A; Ray P; Harper J; Lesko J; Paraschos T; Atkinson G; Soussis I; Taylor D; Handyside A; Hughes M; Winston RM Prenat Diagn; 1996 Feb; 16(2):137-42. PubMed ID: 8650124 [TBL] [Abstract][Full Text] [Related]
15. Improvement of preimplantation genetic diagnosis (PGD) for the cystic fibrosis mutation delta F508 by fluorescent polymerase chain reaction. Moutou C; Viville S Prenat Diagn; 1999 Dec; 19(13):1248-50. PubMed ID: 10660962 [No Abstract] [Full Text] [Related]
16. The ethical context. Prenatal diagnosis of cystic fibrosis and other genetic diseases. Jones CC J Kans Med Soc; 1982 Nov; 83(11):571-8, 592. PubMed ID: 7175326 [No Abstract] [Full Text] [Related]
17. Strategies for the detection of autosomal fetal DNA sequence from maternal peripheral blood. Lo YM; Fleming KA; Wainscoat JS Ann N Y Acad Sci; 1994 Sep; 731():204-13. PubMed ID: 7524389 [No Abstract] [Full Text] [Related]
18. Outcome of intracytoplasmic sperm injection for a couple in which the man is carrier of CFTR p.[R74W;V201M;D1270N] and p.P841R mutations and his spouse a heterozygous carrier of p.F508del mutation of the cystic fibrosis transmembrane conductance regulator gene. Brugnon F; Bilan F; Heraud MC; Grizard G; Janny L; Creveaux I Fertil Steril; 2008 Nov; 90(5):2004.e23-6. PubMed ID: 18703181 [TBL] [Abstract][Full Text] [Related]