1. Tommerup, N. (1993) Mendelian cytogenetics. Chromosome rearrangements associated with mendelian disorders. J. Med. Genet., 30, 713–727.
2. Jacobs, P.A., Hunt, P.A., Mayer, M. and Bart, R.D. (1981) Duchenne muscular dystrophy (DMD) in a female with an X/autosome translocation: further evidence that the DMD locus is at Xp21. Am. J. Hum. Genet., 33, 513–518.
3. Herrera, L., Kakati, S., Gibas, L., Pietrzak, E. and Sandberg, A.A. (1986) Gardner syndrome in a man with an interstitial deletion of 5q. Am. J. Med. Genet., 25, 473–476.
4. Lele, K.P., Penrose, L.S. and Stallard, H.B. (1963) Chromosome deletion in a case of retinoblastoma. Ann. Hum. Genet., 27, 171–174.
5. Riccardi, V.M., Sujansky, E., Smith, A.C. and Francke, U. (1978) Chromosomal imbalance in the Aniridia-Wilms' tumor association: 11p interstitial deletion. Pediatrics, 61, 604–610.