Wendy P. Robinson

The mechanisms involved in formation of deletions and duplications of 15q11-q13.

D. Abeliovich, W. Robinson, R. Nicholls, 1998, Journal of medical genetics.

Sex-specific meiotic recombination in the Prader--Willi/Angelman syndrome imprinted region.

W. Robinson, M. Lalande, Marc Lalande, 1995, Human molecular genetics.

Uniparental disomy explains the occurrence of the Angelman or Prader-Willi syndrome in patients with an additional small inv dup(15) chromosome.

F. Bernasconi, A. Schinzel, Joseph Wagstaff, 1993, Journal of medical genetics.

The origin of abnormalities in recurrent aneuploidy/polyploidy.

W. Robinson, M. Stephenson, D. McFadden, 2001, American journal of human genetics.

Maternal meiosis I non-disjunction of chromosome 15: dependence of the maternal age effect on level of recombination.

D. Ledbetter, S. Christian, S. Schuffenhauer, 1998, Human molecular genetics.

Nondisjunction of chromosome 15: origin and recombination.

D. Ledbetter, S. Langlois, S. Malcolm, 1993, American journal of human genetics.