1. 8p23.1 duplication syndrome; common, confirmed, and novel features in six further patients1. Issue 3 (23rd January 2013) Authors: Barber, John C.K.; Rosenfeld, Jill A.; Foulds, Nicola; Laird, Sophie; Bateman, Mark S.; Thomas, N. Simon; Baker, Samantha; Maloney, Viv K.; Anilkumar, Arayamparambil; Smith, Wendy E.; Banks, Valerie; Ellingwood, Sara; Kharbutli, Yara; Mehta, Lakshmi; Eddleman, Keith A.; Marble, Michael; Zambrano,... Journal: American journal of medical genetics Issue: Volume 161:Issue 3(2013:Mar.) Page Start: 487 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Controversies in prenatal diagnosis 3: should everyone undergoing invasive testing have a microarray?. (January 2014) Authors: Crolla, John A.; Wapner, Ronald; Van Lith, Jan M. M. Journal: Prenatal diagnosis Issue: Volume 34:Number 1(2014:Jan.) Page Start: 18 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. De novo interstitial deletion 2q14.1q22.1: Is there a recognizable phenotype?. Issue 12 (26th September 2014) Authors: Greally, Marie T.; Robinson, Eve; Allen, Nicholas M.; O'Donovan, Donough; Crolla, John A. Journal: American journal of medical genetics Issue: Volume 164:Issue 12(2014.) Page Start: 3194 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Duplication of 17q11.2 and Features of Albright Hereditary Osteodystrophy Secondary to Methylation Defects within the GNAS Cluster: Coincidence or Causal?. (14th January 2013) Authors: White, M.; Conroy, J.; Bullman, H.; Lever, M.; Daly, E.; Betts, D. R.; Cody, D.; Crolla, John A.; Lynch, S. A. Other Names: DeWan A. Academic Editor.; Fenger M. Academic Editor. Journal: Case reports in genetics Issue: Volume 2013(2013) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. The clinical utility of microarray technologies applied to prenatal cytogenetics in the presence of a normal conventional karyotype: a review of the literature. (8th September 2013) Authors: Callaway, Jonathan L. A.; Shaffer, Lisa G.; Chitty, Lyn S.; Rosenfeld, Jill A.; Crolla, John A. Journal: Prenatal diagnosis Issue: Volume 33:Number 12(2013:Dec.) Page Start: 1119 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗