1. Acute lymphoblastic leukemia in a child with a de novo germline gnb1 mutation. Issue 2 (19th October 2016) Authors: Brett, Maggie; Lai, Angeline H. M.; Ting, Teck‐Wah; Tan, Ah‐Moy; Foo, Roger; Jamuar, Saumya; Tan, Ene‐Choo Journal: American journal of medical genetics Issue: Volume 173:Issue 2(2017) Page Start: 550 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Additional individuals with CHD7 variants in Chinese and other southeast Asian patients. Issue 10 (17th August 2020) Authors: Wei, Heming; Tan, Ee‐Shien; Jamuar, Saumya; Lai, Angeline H. M.; Ng, Ivy; Tan, Ene‐Choo Journal: American journal of medical genetics Issue: Volume 182:Issue 10(2020) Page Start: 2461 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Novel phenotypic feature in a patient with a recurrent NOTCH2 nonsense mutation. Issue 7 (15th March 2022) Authors: Tan, Ene‐Choo; Lai, Angeline H. M.; Brett, Maggie S. Y. Journal: American journal of medical genetics Issue: Volume 188:Issue 7(2022) Page Start: 2135 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. The spectrum of genetic variants and phenotypic features of Southeast Asian patients with Noonan syndrome. Issue 4 (19th February 2019) Authors: Koh, Ai‐Ling; Tan, Ee‐Shien; Brett, Maggie S.; Lai, Angeline H. M.; Jamuar, Saumya Shekhar; Ng, Ivy; Tan, Ene‐Choo Journal: Molecular genetics & genomic medicine Issue: Volume 7:Issue 4(2019) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗