au.\*:("FODOR, F. H")
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Selection :
Frequency and carrier risk associated with common BRCA1 and BRCA2 mutations in Ashkenazi Jewish breast cancer patientsFODOR, F. H; WESTON, A; BLEIWEISS, I. J et al.American journal of human genetics. 1998, Vol 63, Num 1, pp 45-51, issn 0002-9297Article
A dinucleotide repeat polymmorphism at the DMD locusPOWELL, J. F; FODOR, F. H; COCKBURN, D. J et al.Nucleic acids research. 1991, Vol 19, Num 5, issn 0305-1048, p. 1159Article
Molecular exclusion of Haemoglobin SD disease by prenatal diagnosisFODOR, F. H; ENG, C. M.Prenatal diagnosis. 1999, Vol 19, Num 1, pp 58-60, issn 0197-3851Article