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.
111 related articles for article (PubMed ID: 1700249)
1. Prenatal screening for delta F508 mutation in population not selected for cystic fibrosis. Bick D; Maddalena A; Black SH; Headrick EG; Cummings E; Jones SL; Costakos D; Becker R; Schulman JD Lancet; 1990 Nov; 336(8726):1324-5. PubMed ID: 1700249 [No Abstract] [Full Text] [Related]
2. The delta F508 mutation in mild adult forms of cystic fibrosis (CF). Simon-Bouy B; Mornet E; Taillandier A; Serre JL; Boue J; Boue A Clin Genet; 1991 Apr; 39(4):304-5. PubMed ID: 1712680 [TBL] [Abstract][Full Text] [Related]
3. Optimal polymerase chain reaction amplification for preimplantation diagnosis in cystic fibrosis (delta F508). Cui KH; Haan EA; Wang LJ; Matthews CD BMJ; 1995 Aug; 311(7004):536-40. PubMed ID: 7545043 [TBL] [Abstract][Full Text] [Related]
4. Characterization of the frequency of delta F508 mutation and CF haplotypes in Swedish families. Anvret M; Stolpe L; Dahl N; Eiserman M; Nordenskjöld M; Starborg M; Johansson L Clin Genet; 1991 Mar; 39(3):238-9. PubMed ID: 1709843 [No Abstract] [Full Text] [Related]
5. Cystic fibrosis mutations delta F508 and G542X in Jewish patients. Lerer I; Sagi M; Cutting GR; Abeliovich D J Med Genet; 1992 Feb; 29(2):131-3. PubMed ID: 1377276 [TBL] [Abstract][Full Text] [Related]
6. Analysis of delta F508 mutation in cystic fibrosis pathology specimens. Ozgüç M; Tekin A; Erdem H; Yilmaz E; Ayter S; Coşkun T; Can A; Gögüş S; Caglar M; Kale G Pediatr Pathol; 1994; 14(3):491-6. PubMed ID: 7520582 [TBL] [Abstract][Full Text] [Related]
7. Frequency of delta F508 mutation and haplotype analysis in Austrian cystic fibrosis families. Larsen J; Georghiou A; Kury FD; Götz M; Sanz K; Dobianer K; Spona J Hum Genet; 1992 Jun; 89(4):464-5. PubMed ID: 1377660 [No Abstract] [Full Text] [Related]
8. Preimplantation diagnosis of cystic fibrosis by simultaneous detection of the W1282X and delta F508 mutations. Avner R; Laufer N; Safran A; Kerem BS; Friedmann A; Mitrani-Rosenbaum S Hum Reprod; 1994 Sep; 9(9):1676-80. PubMed ID: 7530726 [TBL] [Abstract][Full Text] [Related]
9. Birth of a normal girl after in vitro fertilization and preimplantation diagnostic testing for cystic fibrosis. Handyside AH; Lesko JG; Tarín JJ; Winston RM; Hughes MR N Engl J Med; 1992 Sep; 327(13):905-9. PubMed ID: 1381054 [TBL] [Abstract][Full Text] [Related]
10. Genetic analysis of cystic fibrosis. Estivill X; Casals T; Nunes V Adv Exp Med Biol; 1991; 290():31-8. PubMed ID: 1719767 [No Abstract] [Full Text] [Related]
11. The delta F508 mutation and RFLP-linked loci in Spanish cystic fibrosis families. Peral B; Hernández-Chico C; San Millán JL; Granell R; Molano J; Carrasco S; Tellería JJ; Devoto M; Moreno F Hum Genet; 1991 Aug; 87(4):516-7. PubMed ID: 1715312 [No Abstract] [Full Text] [Related]
12. Neonatal screening for the cystic fibrosis main mutation delta F508 in Estonia. Klaassen T; Teder M; Viikmaa M; Metspalu A J Med Screen; 1998; 5(1):16-9. PubMed ID: 9575453 [TBL] [Abstract][Full Text] [Related]
13. Mutation analysis and haplotype correlation for 139 cystic fibrosis patients from the Nebraska Regional Cystic Fibrosis Center. Traystman MD; Schulte N; Colombo JL; Sammut PH; Reilly P; Patel C; Acquazzino D; Simanek B; Anderson R; Kimberling WJ Hum Mutat; 1993; 2(1):7-15. PubMed ID: 7682884 [TBL] [Abstract][Full Text] [Related]
14. Mutation analysis in 600 French cystic fibrosis patients. Chevalier-Porst F; Bonardot AM; Gilly R; Chazalette JP; Mathieu M; Bozon D J Med Genet; 1994 Jul; 31(7):541-4. PubMed ID: 7525963 [TBL] [Abstract][Full Text] [Related]
15. Altered chloride ion channel kinetics associated with the delta F508 cystic fibrosis mutation. Dalemans W; Barbry P; Champigny G; Jallat S; Dott K; Dreyer D; Crystal RG; Pavirani A; Lecocq JP; Lazdunski M Nature; 1991 Dec 19-26; 354(6354):526-8. PubMed ID: 1722027 [TBL] [Abstract][Full Text] [Related]
16. The direct early diagnosis of cystic fibrosis by the detection of the delta F508 CFTR gene mutation in a prematurely delivered boy. Macek M; Macek M; Stuhrmann M; Kulovaný E; Dolanská M; Koukolík F; Boehm I; Hronková J; Jezková Z; Paulová M Clin Genet; 1991 Mar; 39(3):219-22. PubMed ID: 1709842 [TBL] [Abstract][Full Text] [Related]
17. [Molecular-genetic analysis of certain mutations of the "cystic fibrosis gene" in Moldavia. Characteristics of molecular markers and their linkage with various mutations]. Gimbovskaia SD; Kalinin VN; Ivashchenko TE; Baranov VS Genetika; 1994 Dec; 30(12):1616-20. PubMed ID: 7534245 [TBL] [Abstract][Full Text] [Related]
19. Prenatal diagnosis of cystic fibrosis in a highly heterogeneous population. Casals T; Gimenez J; Ramos MD; Nunes V; Estivill X Prenat Diagn; 1996 Mar; 16(3):215-22. PubMed ID: 8710774 [TBL] [Abstract][Full Text] [Related]
20. [A molecular study of the delta-F508 mutation and genetic analysis of a sample of cystic fibrosis patients]. Orozco L; Lezana JL; Chávez M; Valdez H; Moreno M; Carnevale A Bol Med Hosp Infant Mex; 1993 Jul; 50(7):457-62. PubMed ID: 7689846 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]