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6. Genetics of neurofibromatosis 1 in Japan: mutation rate and paternal age effect. Takano T; Kawashima T; Yamanouchi Y; Kitayama K; Baba T; Ueno K; Hamaguchi H Hum Genet; 1992 May; 89(3):281-6. PubMed ID: 1351032 [TBL] [Abstract][Full Text] [Related]
7. Molecular analysis of cystic fibrosis in the Hungarian population. Nemeti M; Louie E; Papp Z; Johnson JP Hum Genet; 1991 Aug; 87(4):511-2. PubMed ID: 1715311 [TBL] [Abstract][Full Text] [Related]
8. 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]
9. A cystic fibrosis patient with delta F508, G542X and a deletion at the D7S8 locus. Wagner K; Greil I; Schneditz P; Pommer M; Rosenkranz W Hum Mutat; 1994; 3(3):327-9. PubMed ID: 7517267 [No Abstract] [Full Text] [Related]
10. Approaches to localizing disease genes as applied to cystic fibrosis. Dean M; Drumm ML; Stewart C; Gerrard B; Perry A; Hidaka N; Cole JL; Collins FS; Iannuzzi MC Nucleic Acids Res; 1990 Jan; 18(2):345-50. PubMed ID: 1970161 [TBL] [Abstract][Full Text] [Related]
11. A de novo cystic fibrosis mutation: CGA (Arg) to TGA (stop) at codon 851 of the CFTR gene. White MB; Leppert M; Nielsen D; Zielenski J; Gerrard B; Stewart C; Dean M Genomics; 1991 Nov; 11(3):778-9. PubMed ID: 1723056 [No Abstract] [Full Text] [Related]
12. Absence of linkage of Noonan syndrome to the neurofibromatosis type 1 locus. Sharland M; Taylor R; Patton MA; Jeffery S J Med Genet; 1992 Mar; 29(3):188-90. PubMed ID: 1348095 [TBL] [Abstract][Full Text] [Related]
13. A rare DNA variant in exon 15 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene. Chillón M; Palacio A; Nunes V; Estivill X Hum Genet; 1992 Dec; 90(4):474. PubMed ID: 1282900 [No Abstract] [Full Text] [Related]
14. Diagnosis of neurofibromatosis type 1 using RFLPs tightly linked to gene. Vivarelli R; Bartalani G; Berardi A; Calistri L; Balestri P; Fois A Childs Nerv Syst; 1993 Jun; 9(3):147-9. PubMed ID: 8104099 [TBL] [Abstract][Full Text] [Related]
15. Utility of internal markers to improve the accuracy of cystic fibrosis genotype analysis. Raskin S; Phillips JA; Vnencak-Jones C; Dawson E; Kaplan G; McClure M Biotechniques; 1992 Sep; 13(3):372-4. PubMed ID: 1382468 [TBL] [Abstract][Full Text] [Related]
16. Patterns of polymorphism and linkage disequilibrium for cystic fibrosis. Estivill X; Scambler PJ; Wainwright BJ; Hawley K; Frederick P; Schwartz M; Baiget M; Kere J; Williamson R; Farrall M Genomics; 1987 Nov; 1(3):257-63. PubMed ID: 2895728 [TBL] [Abstract][Full Text] [Related]
17. The gene for congenital chloride diarrhea maps close to but is distinct from the gene for cystic fibrosis transmembrane conductance regulator. Kere J; Sistonen P; Holmberg C; de la Chapelle A Proc Natl Acad Sci U S A; 1993 Nov; 90(22):10686-9. PubMed ID: 7504277 [TBL] [Abstract][Full Text] [Related]
18. [Molecular biological analysis of cystic fibrosis--a model example for the strategy of "reverse genetics"]. Coutelle C; Grade K Padiatr Grenzgeb; 1992; 31(2):73-95. PubMed ID: 1284810 [TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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] [Next] [New Search]