1. Aldridge J, Kunkel LM, Bruns G, Tantravahi U, Lalond M, Brenster T, Moreau E, Wilson M, Bromley W, Rodrick T, Latt SA (1984) A strategy to reveal high frequence RFLPs along the human X chromosome. Am J Hum Genet 36: 546?564
2. Ashley T (1983) Sex vesicle loss: a possible explanation of the excess of X0 over XXY conceptuses in mice and men. Hum Genet 65: 209?210
3. Bakker E, Hofker MH, Goor N, Mandel JL, Wrogemann K, Davies KE, Kunkel LM, Willard HF, Fenton WA, Sankuyl L, Majoor-Krakauer D, van Essen AJ, Jahoda MJG, Sachs ES, van Ommen GJB, Pearson PL (1985) Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy with closely linked RFLPs. Lancet II: 655?658
4. Bjerlund-Nielsen L, Nielsen IM (1984) Turner's syndrome and Duchenne muscular dystrophy in a girl with an X: autosome translocation. Ann Genet (Paris) 27: 173?177
5. Dutrillaux B, Lejeune J (1971) Sur une nouvelle technique d'analyse du caryotype humain. C R Acad Sci Paris, Sér D, 272: 2638?2640