S. O’Donnell

Randomized trial of a decision aid for individuals considering genetic testing for hereditary nonpolyposis colorectal cancer risk

Judi Homewood, Claire E Wakefield, Robyn Ward, 2008, Cancer.

Computer face-matching technology using two-dimensional photographs accurately matches the facial gestalt of unrelated individuals with the same syndromic form of intellectual disability

B. D. de Vries, B. Lovell, H. Brunner, 2017, BMC Biotechnology.

Clinical report: one year of treatment of Proteus syndrome with miransertib (ARQ 092)

L. Biesecker, B. Schwartz, Paula Doherty, 2020, Cold Spring Harbor molecular case studies.

A Familial 7 q 36 . 3 Duplication Associated with Agenesis of the Corpus Callosum

B. Kamien, S. O’Donnell, R. Moldrich, 2015 .

A familial 7q36.3 duplication associated with agenesis of the corpus callosum

B. Kamien, S. O’Donnell, R. Moldrich, 2015, American journal of medical genetics. Part A.

Narrowing the critical region for overgrowth within 13q14.2-q14.3 microdeletions.

R. Scott, M. Digilio, C. Meldrum, 2015, European journal of medical genetics.

An intragenic deletion of the NFIA gene in a patient with a hypoplastic corpus callosum, craniofacial abnormalities and urinary tract defects.

C. Meldrum, S. O’Donnell, Anupam Rao, 2014, European journal of medical genetics.