doi.org/10.1086/302703, hdl.handle.net/1765/59356
American Journal of Human Genetics
Department of Clinical Genetics

Holinski-Feder, E., Reyniers, E., Uhrig, S., Golla, A., Wauters, J., Kroisel, P., Bossuyt, P., Rost, J., Jedele, K., Zierler, H., Schwab, S., Wildenauer, D., Speicher, M., Willems, P., Meitinger, T.& Kooy, F. (2000). Familial mental retardation syndrome ATR-16 due to an inherited cryptic subtelomeric translocation, t(3;16)(q29;p13.3). American Journal of Human Genetics, 66(1), 16–25.https://doi.org/10.1086/302703