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.
110 related articles for article (PubMed ID: 2903315)
1. Prenatal diagnosis of cystic fibrosis where single affected child has died: Guthrie spots and microvillar enzyme testing. McIntosh I; Strain L; Brock DJ Lancet; 1988 Nov; 2(8619):1085. PubMed ID: 2903315 [No Abstract] [Full Text] [Related]
2. [Prenatal diagnosis of cystic fibrosis by analysis of microvillar enzymes of the amniotic fluid]. Szabó M; Teichmann F; Huszka M; Münnich A; Veress L; Papp Z Orv Hetil; 1990 Aug; 131(32):1749-50, 1753-5. PubMed ID: 2205827 [TBL] [Abstract][Full Text] [Related]
3. Two unusual cases of first trimester prenatal diagnosis of cystic fibrosis using DNA probes. Law HY; Stanier P; Williamson R; Modell B; Ward RH; Petrou M; Old J; Farrall M Prenat Diagn; 1987 Mar; 7(3):215-21. PubMed ID: 3588540 [TBL] [Abstract][Full Text] [Related]
4. First-trimester prenatal diagnosis of cystic fibrosis with linked DNA probes. Farrall M; Law HY; Rodeck CH; Warren R; Stanier P; Super M; Lissens W; Scambler P; Watson E; Wainwright B Lancet; 1986 Jun; 1(8495):1402-5. PubMed ID: 2872515 [TBL] [Abstract][Full Text] [Related]
5. First trimester diagnosis of Hunter syndrome on chorionic villi. Kleijer WJ; van Diggelen OP; Janse HC; Galjaard H; Dumez Y; Boué J Lancet; 1984 Aug; 2(8400):472. PubMed ID: 6147543 [No Abstract] [Full Text] [Related]
7. Molecular screening of cystic fibrosis patients. Fellowes AP; Murphy JM; Wesley AW; Dawson KP; George PM N Z Med J; 1991 Oct; 104(921):415-6. PubMed ID: 1923090 [TBL] [Abstract][Full Text] [Related]
8. Prenatal diagnosis of cystic fibrosis using linked DNA markers and microvillar intestinal enzyme analysis. Spence JE; Buffone GJ; Rosenbloom CL; Fernbach SD; Curry MR; Carpenter RJ; Ledbetter DH; O'Brien WE; Beaudet AL Hum Genet; 1987 May; 76(1):5-10. PubMed ID: 3471704 [TBL] [Abstract][Full Text] [Related]
9. Prenatal diagnosis of hereditary tyrosinaemia type I by determination of fumarylacetoacetase in chorionic villus material. Kvittingen EA; Guibaud PP; Divry P; Mandon G; Rolland MO; Domenichini Y; Jakobs C; Christensen E Eur J Pediatr; 1986 Apr; 144(6):597-8. PubMed ID: 3709578 [No Abstract] [Full Text] [Related]
10. Prenatal diagnosis of cystic fibrosis in a Turkish family. Yilmaz E; Ozgüç M; Coşkun T; Beksaç S; Cakar N; Ayter S; Ozalp I Turk J Pediatr; 1991; 33(2):79-84. PubMed ID: 1844185 [TBL] [Abstract][Full Text] [Related]
11. Prenatal diagnosis of cystic fibrosis by chorionic villus sampling using 12 polymorphic deoxyribonucleic acid markers. Nugent CE; Gravius T; Green P; Larsen JW; MacMillin MD; Donis-Keller H Obstet Gynecol; 1988 Feb; 71(2):213-5. PubMed ID: 3422111 [TBL] [Abstract][Full Text] [Related]
12. Prenatal diagnosis of cystic fibrosis by microvillar membrane enzyme analysis in amniotic fluid. Szabó M; Teichmann F; Huszka M; Münnich A; Veress L; Papp Z Acta Paediatr Hung; 1991; 31(2):263-74. PubMed ID: 1867893 [TBL] [Abstract][Full Text] [Related]
13. Use of linkage disequilibrium data in prenatal diagnosis of cystic fibrosis. Strain L; Curtis A; Mennie M; Holloway S; Brock DJ Hum Genet; 1988 Sep; 80(1):75-7. PubMed ID: 3417307 [TBL] [Abstract][Full Text] [Related]
14. Feasibility of first trimester prenatal diagnosis of Hunter syndrome. Lykkelund C; Søndergaard F; Therkelsen AJ; Tønnesen T; Rasmussen V; Mikkelsen M; Güttler F; Nyland MH Lancet; 1983 Nov; 2(8359):1147. PubMed ID: 6138678 [No Abstract] [Full Text] [Related]
15. 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]
16. [Prenatal diagnosis of cystic fibrosis]. ten Kate LP Tijdschr Kindergeneeskd; 1987 Apr; 55(2):53-63. PubMed ID: 2884752 [TBL] [Abstract][Full Text] [Related]
17. First-trimester prenatal diagnosis of cystic fibrosis using fibroblasts from a deceased index child to establish haplotypes. Curtis A; Strain L; Mennie M; Holloway S; Raeburn JA; Besley GT; Brock DJ Prenat Diagn; 1988 Oct; 8(8):625-8. PubMed ID: 3205866 [TBL] [Abstract][Full Text] [Related]
18. Clinic experience of prenatal diagnosis of cystic fibrosis by use of linked DNA probes. Super M; Ivinson A; Schwarz M; Giles L; Elles RG; Read AP; Harris R Lancet; 1987 Oct; 2(8562):782-4. PubMed ID: 2888995 [TBL] [Abstract][Full Text] [Related]
19. Results of second trimester prenatal diagnosis of cystic fibrosis in risk families. Vávrová V; Thomásová H; Macek M Czech Med; 1989; 12(2):96-100. PubMed ID: 2569963 [TBL] [Abstract][Full Text] [Related]
20. Prenatal diagnosis of cystic fibrosis by assay of amniotic fluid microvillar enzymes. Brock DJ; Bedgood D; Hayward C Hum Genet; 1984; 65(3):248-51. PubMed ID: 6141994 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]