Frequent chromosome aberrations revealed by molecular cytogenetic studies in patients with aniridia

by Crolla, John A., van Heyningen, Veronica
Published 2002

Supernumerary marker chromosomes in man: parental origin, mosaicism and maternal age revisited

by Crolla, John A., Youings, Sheila A., Ennis, Sarah, Jacobs, Patricia A.
Published 2005

Evaluation of a novel assay for detection of the fetal marker RASSF1A: facilitating improved diagnostic reliability of noninvasive prenatal diagnosis

by Oudejans, Cees, White, Helen E., Dent, Carolyn L., Hall, Victoria J., Crolla, John A., Chitty, Lyn S.
Published 2012

Failure to find DUP25 in patients with anxiety disorders, in control individuals, or in previously reported positive control cell lines

by Tabiner, Melody, Youings, Sheila, Dennis, Nicholas, Baldwin, David, Buis, Christel, Mayers, Andrew, Jacobs, Patricia A., Crolla, John A.
Published 2003

A novel class of pseudoautosomal region 1 deletions downstream of SHOX is associated with Léri-Weill dyschondrosteosis

by Benito-Sanz, Sara, Thomas, N. Simon, Huber, Céline, del Blanco, Darya Gorbenko, Aza-Carmona, Miriam, Crolla, John A., Maloney, Vivienne, Argente, Jesús, Campos-Barros, Ángel, Cormier-Daire, Valérie, Heath, Karen E.
Published 2005

Clinical and molecular characterization of the 20q11.2 microdeletion syndrome: Six new patients

by Jedraszak, Guillaume, Demeer, Bénédicte, Mathieu-Dramard, Michèle, Andrieux, Joris, Receveur, Aline, Weber, Astrid, Maye, Una, Foulds, Nicola, Temple, IK, Crolla, John, Alex-Cordier, Sanlaville, Damien, Ewans, Lisa, Wilson, Meredith, Armstrong, Ruth, Clarkson, Amanda, Copin, Henri, Morin, Gilles
Published 2015