Prenatal screening for cystic fibrosis
De Braekeleer, M.
Lancet 343(8890): 172-173
1994
ISSN/ISBN: 0140-6736 PMID: 7904016 Document Number: 429847
Document emailed within 1 workday
Related Documents
Kampmann, W.; Mathy, L.; Grzeschik, K.H.; Driesel, A.j.; Bartholomé, K.; Neugebauer, M.; Olek, K. 1989: Prenatal diagnosis of cystic fibrosis Journal of Clinical Chemistry and Clinical Biochemistry 27(3): 117-122Schmidtke, J.; Krawczak, M. 1987: Prenatal diagnosis of cystic fibrosis with recombinant DNA methods Monatsschrift Kinderheilkunde: Organ der Deutschen Gesellschaft für Kinderheilkunde 135(12): 805-810
Demay, G.; Stubnicer, A.C.; Boué, A.; Boué, J.; Pechevis, M.; Lenoir, G. 1986: Requests for prenatal diagnosis from parents of children with cystic fibrosis Journal de Genetique Humaine 34(3-4): 235-243
Voss, R.; Hertz, B.; Chemke, J.; Katznelson, D.; Yahav, Y. 1988: Cystic fibrosis: linked DNA markers in prenatal diagnosis and carrier detection Harefuah 114(7): 317-320
Seale, T.W.; Rennert, O.M. 1982: Current status of prenatal diagnosis and heterozygote detection of cystic fibrosis Annals of Clinical and Laboratory Science 12(5): 415-423
Sedlácek, Z.; Macek, M.; Hronková, J.; Tomásová, H.; Chudoba, D.; Vávrová, V. 1990: Strategies in prenatal diagnosis of cystic fibrosis after the introduction of DNA analysis. Initial experience Casopis Lekaru Ceskych 129(22): 683-688
Baiget, M.; Casals, T.; Nunes, V.; Estivill, X. 1989: Detection of carriers and prenatal diagnosis of cystic fibrosis in Spanish families using DNA markers Medicina Clinica 92(10): 361-363
Rosenstein, B.J.; Langbaum, T.S. 1983: Screening for cystic fibrosis JAMA 249(23): 3175
Lyon, I.C.; Crossley, J.R.; Smith, P.A. 1983: Screening for cystic fibrosis New Zealand Medical Journal 96(739): 673-675
Boué, J.; Muller, F.; Simon-Bouy, B.; Faure, C.; Boué, A. 1991: Consequences of prenatal diagnosis of cystic fibrosis on the reproductive attitudes of parents of affected children Prenatal Diagnosis 11(4): 209-214
Novelli, G.; Mannello, F.; Pierotti, C.; Antonelli, M.; Dallapiccola, B. 1988: Protocol for prenatal diagnosis of cystic fibrosis based on studies of alkaline phosphatase isoenzymes Journal of Laboratory and Clinical Medicine 112(2): 201-207
Casals Senent, T.; Nunes Martínez, V.; Giménez Gasco, J.; Parra Roca, J.; Estivill Palleja, X. 1990: Prenatal diagnosis of cystic fibrosis, using DNA markers, in Spanish families: experience during 1987-1989 Anales Espanoles de Pediatria 32(4): 287-292
Lyon, I.C.; Webster, D.R. 1991: Newborn screening for cystic fibrosis Pediatrics 87(6): 954-956
Brock, D.J. 1996: Cost effectiveness of antenatal screening for cystic fibrosis. Realistic cost must be established for genetic counselling in two step screening Bmj 312(7035): 908; Author Reply 910
Nugent, C.E.; Gravius, T.; Green, P.; Larsen, J.W.; MacMillin, M.D.; Donis-Keller, H. 1988: Prenatal diagnosis of cystic fibrosis by chorionic villus sampling using 12 polymorphic deoxyribonucleic acid markers Obstetrics and Gynecology 71(2): 213-215
Brandt, N.J.; Schwartz, M.; Skovby, F. 1991: Orientation on genetic screening for cystic fibrosis Ugeskrift for Laeger 153(19): 1365-1368
Uxa, F.; Marchi, A.G. 1979: Screening for cystic fibrosis in the newborn infant Minerva Pediatrica 31(11): 831-833
1976: Screening newborn infants for cystic fibrosis Medical Letter on Drugs and Therapeutics 18(8): 35-36
Fellowes, A.P.; Murphy, J.M.; Wesley, A.W.; Dawson, K.P.; George, P.M. 1991: Molecular screening of cystic fibrosis patients New Zealand Medical Journal 104(921): 415-416
Denter, M.; Ramsay, M.; Jenkins, T. 1992: Cystic fibrosis. Part I. Frequency of the delta F508 mutation in South African families with cystic fibrosis South African Medical Journal 82(1): 7-10