J. Macfarlane

Y chromosome specific probes identify breakpoint in a 45,X/46,X,del(Y)(pter----q11.1:) karyotype of an infertile male.

P. Goodfellow, G. Beverstock, H. Veenema, 1989, Journal of medical genetics.

Parental origin of a ring 13 chromosome in a female with multiple anomalies

R. Magenis, H. Wyandt, K. Overton, 1976, Human Genetics.

Interstitial deletion of (17)(p11.2p11.2) in nine patients.

J. Opitz, J. Reiss, L. Mcgavran, 1986, American journal of medical genetics.

Comparison of the 15q deletions in Prader-Willi and Angelman syndromes: specific regions, extent of deletions, parental origin, and clinical consequences.

J. Zonana, S. Lafranchi, R. Magenis, 1990, American journal of medical genetics.