1. 8p23.2p22 deletion: a case report of a large deletion encompassing 8p23.1 with additional clinical features. Issue 4 (October 2020) Authors: LaBranche, Jennifer T.N.; Argiropoulos, Bob; Thomas, Mary Ann Journal: Clinical dysmorphology Issue: Volume 29:Issue 4(2020:Oct.) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Atypical Prenatal Ultrasound Presentation and Neuropathological Findings in a Neonate With Alpha Thalassemia Major: A Case Report. (March 2019) Authors: Chan, Elaine S; Lauzon, Julie; Resch, Lothar; Argiropoulos, Bob; Schmitt, Laura; Chadha, Rati Journal: Pediatric and developmental pathology Issue: Volume 22:Number 2(2019) Page Start: 166 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Authors' Response: Prenatal Ultrasound Presentations in Late Pregnancies Affected With Alpha Thalassemia Major. (December 2019) Authors: Chan, Elaine S; Lauzon, Julie; Resch, Lothar; Argiropoulos, Bob; Schmitt, Laura; Chadha, Rati Journal: Pediatric and developmental pathology Issue: Volume 22:Number 6(2019) Page Start: 605 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Congenital hiatal hernia segregating with a duplication in 9q22.31q22.32 in two families. Issue 12 (7th October 2020) Authors: Chang, Caitlin A.; Di Donato, Nataliya; Hackmann, Karl; Argiropoulos, Bob; Ferreira, Patrick; Innes, A. Micheil; Thomas, Mary Ann Journal: American journal of medical genetics Issue: Volume 182:Issue 12(2020) Page Start: 3040 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Genotype–phenotype characterization in 13 individuals with chromosome Xp11.22 duplications. Issue 4 (22nd December 2015) Authors: Grams, Sarah E.; Argiropoulos, Bob; Lines, Matthew; Chakraborty, Pranesh; Mcgowan‐Jordan, Jean; Geraghty, Michael T.; Tsang, Marilyn; Eswara, Marthand; Tezcan, Kamer; Adams, Kelly L.; Linck, Leesa; Himes, Patricia; Kostiner, Dana; Zand, Dina J.; Stalker, Heather; Driscoll, Daniel J.; Huang, Taosh... Journal: American journal of medical genetics Issue: Volume 170:Issue 4(2016) Page Start: 967 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. MG-127 Residual disease monitoring in a retinoblastoma patient by pcr of a novel deletion breakpoint. (4th December 2015) Authors: Corson, Tim; Racher, Hilary; Argiropoulos, Bob; Chan, Helen; Perrier, Renée; Matevski, Donco; Rushlow, Diane; Shaikh, Furqan; Trang, Heather; Gallie, Brenda Journal: Journal of medical genetics Issue: Volume 52(2015)Supplement 2 Page Start: A10 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Optimized serial expansion of human induced pluripotent stem cells using low-density inoculation to generate clinically relevant quantities in vertical-wheel bioreactors. (22nd May 2020) Authors: Borys, Breanna S.; So, Tania; Colter, James; Dang, Tiffany; Roberts, Erin L.; Revay, Tamas; Larijani, Leila; Krawetz, Roman; Lewis, Ian; Argiropoulos, Bob; Rancourt, Derrick E.; Jung, Sunghoon; Hashimura, Yas; Lee, Brian; Kallos, Michael S. Journal: Stem cells translational medicine Issue: Volume 9:Number 9(2020) Page Start: 1036 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Optimized serial expansion of human induced pluripotent stem cells using low‐density inoculation to generate clinically relevant quantities in vertical‐wheel bioreactors. (22nd May 2020) Authors: Borys, Breanna S.; So, Tania; Colter, James; Dang, Tiffany; Roberts, Erin L.; Revay, Tamas; Larijani, Leila; Krawetz, Roman; Lewis, Ian; Argiropoulos, Bob; Rancourt, Derrick E.; Jung, Sunghoon; Hashimura, Yas; Lee, Brian; Kallos, Michael S. Journal: Stem cells translational medicine Issue: Volume 9:Number 9(2020) Page Start: 1036 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Refinement of the critical region of 1q41q42 microdeletion syndrome identifies FBXO28 as a candidate causative gene for intellectual disability and seizures. Issue 2 (19th December 2013) Authors: Au, P.Y. Billie; Argiropoulos, Bob; Parboosingh, Jillian S.; Micheil Innes, A. Journal: American journal of medical genetics Issue: Volume 164:Issue 2(2014.) Page Start: 441 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗