1. Are all chromosome microarrays the same? What clinicians need to know. (10th February 2019) Authors: Levy, Brynn; Burnside, Rachel D. Journal: Prenatal diagnosis Issue: Volume 39:Number 3(2019) Page Start: 157 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Features of Feingold syndrome 1 dominate in subjects with 2p deletions including MYCN. Issue 9 (8th August 2018) Authors: Burnside, Rachel D.; Molinari, Sharon; Botti, Christina; Brooks, Susan Sklower; Chung, Wendy K.; Mehta, Lakshmi; Schwartz, Stuart; Papenhausen, Peter Journal: American journal of medical genetics Issue: Volume 176:Issue 9(2018) Page Start: 1956 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Partial monosomy of 11q22.2q22.3 including the SDHD gene in individuals with developmental delay. (3rd March 2015) Authors: Yelavarthi, Krishna; Cabral, Huong; Wilson, Golder N.; Rohena, Luis; Risheg, Hiba; Penton, Andrea; Schleede, Justin; Burnside, Rachel D. Journal: American journal of medical genetics Issue: Volume 167:Number 4(2015:Apr.) Page Start: 695 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Prenatal diagnosis of two fetuses with deletions of 8p23.1, critical region for congenital diaphragmatic hernia and heart defects. Issue 7 (21st May 2013) Authors: Keitges, Elisabeth A.; Pasion, Romela; Burnside, Rachel D.; Mason, Carla; Gonzalez‐Ruiz, Antonio; Dunn, Teresa; Masiello, Meredith; Gebbia, Joseph A.; Fernandez, Carlos O.; Risheg, Hiba Journal: American journal of medical genetics Issue: Volume 161:Issue 7(2013:Jul.) Page Start: 1755 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Recurrent deletions and duplications of chromosome 2q11.2 and 2q13 are associated with variable outcomes. (31st July 2015) Authors: Riley, Kacie N.; Catalano, Lisa M.; Bernat, John A.; Adams, Stacie D.; Martin, Donna M.; Lalani, Seema R.; Patel, Ankita; Burnside, Rachel D.; Innis, Jeffrey W.; Rudd, M. Katharine Journal: American journal of medical genetics Issue: Volume 167:Number 11(2015:Nov.) Page Start: 2664 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Three cases of isolated terminal deletion of chromosome 8p without heart defects presenting with a mild phenotype1. Issue 4 (12th March 2013) Authors: Burnside, Rachel D.; Pappas, John G.; Sacharow, Stephanie; Applegate, Carolyn; Hamosh, Ada; Gadi, Inder K.; Jaswaney, Vikram; Keitges, Elisabeth; Phillips, Karen K.; Potluri, Venketaswara R.; Risheg, Hiba; Smith, Janice L.; Tepperberg, Jim H.; Schwartz, Stuart; Papenhausen, Peter Journal: American journal of medical genetics Issue: Volume 161:Issue 4(2013:Apr.) Page Start: 822 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗