M. Pearson

Clinical spectrum associated with recurrent genomic rearrangements in chromosome 17q12

P. Stankiewicz, E. Roeder, S. Cheung, 2010, European Journal of Human Genetics.

A five generation family with a novel mutation in FOXC2 and lymphedema worsening to hydrops in the youngest generation

R. Erickson, M. Witte, C. Sargent, 2014, American journal of medical genetics. Part A.

Maternal translocation (9;18) with two abnormal offspring each with different chromosome derivatives.

J. Allanson, C. Riske, M. Pearson, 1989, Journal of medical genetics.