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6. Frequency of the phenylalanine deletion (delta F508) in the CF gene of Belgian cystic fibrosis patients. Wauters JG, Hendrickx J, Coucke P, Vits L, Stuer K, van Schil L, van der Auwera BJ, Van Elsen A, Dumon J, Willems PJ. Clin Genet; 1991 Feb; 39(2):89-92. PubMed ID: 1673094 [Abstract] [Full Text] [Related]
7. Cystic fibrosis. Part I. Frequency of the delta F508 mutation in South African families with cystic fibrosis. Denter M, Ramsay M, Jenkins T. S Afr Med J; 1992 Jul; 82(1):7-10. PubMed ID: 1641732 [Abstract] [Full Text] [Related]
8. [The delta F508 mutation which causes cystic fibrosis and its association with closely linked DNA polymorphisms in the Slovak population]. Kádasi L, Gécz J, Puliti A, Devoto M, Ferák V, Romeo G, Kayserová H, Kardosová A, Hruskovic I. Bratisl Lek Listy; 1992 Mar; 93(3):141-5. PubMed ID: 1356071 [Abstract] [Full Text] [Related]
12. [Analysis of various polymorphic markers of the CFTR gene in cystic fibrosis patients and healthy donors from the Moscow region]. Amosenko FA, Sazonova MA, Kapranov NI, Trubnikova IS, Kalinin VN. Genetika; 1995 Apr; 31(4):532-5. PubMed ID: 7607440 [Abstract] [Full Text] [Related]
15. delta F508 frequency and associated haplotypes near the cystic fibrosis locus in the Yugoslav population. Simova L, Williams C, Efremov GD, Gordova-Muratovska A, Sustić S, Watson EK, Williamson R. Hum Genet; 1990 Sep; 85(4):432-3. PubMed ID: 1976597 [Abstract] [Full Text] [Related]
18. [DNA analysis and prenatal diagnosis in cystic fibrosis]. Schnedl W, Weipoltshammer K. Wien Klin Wochenschr; 1991 Sep; 103(2):29-33. PubMed ID: 2024525 [Abstract] [Full Text] [Related]
19. Cystic fibrosis typing with DNA probes and screening for delta F508 deletion in families from southern France. Claustres M, Desgeorges M, Kjellberg P, Bellet H, Demaille J, Ramsay M. Hum Genet; 1990 Sep; 85(4):398-9. PubMed ID: 1976591 [Abstract] [Full Text] [Related]
20. Identification of carriers by screening for delta F508 deletion in a multi-generation cystic fibrosis family. Claustres M, Desgeorges M, Kjellberg P, Demaille J. Genet Couns; 1990 Sep; 1(3-4):211-7. PubMed ID: 1982988 [Abstract] [Full Text] [Related] Page: [Next] [New Search]