1. 8th Australasian Gene Therapy Society Meeting. (20th September 2013) Journal: Journal of gene medicine Issue: Volume 15:Number 8/9(2013:Aug./Sep.) Page Start: 311 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A brief introduction of meta‐analyses in clinical practice and research. (25th March 2021) Authors: Wang, Xiao‐Meng; Zhang, Xi‐Ru; Li, Zhi‐Hao; Zhong, Wen‐Fang; Yang, Pei; Mao, Chen Journal: Journal of gene medicine Issue: Volume 23:Number 5(2021) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. A clinical guidance to DFNA22 drawn from a Korean cohort study with an autosomal dominant deaf population: A retrospective cohort study. (30th April 2018) Authors: Kim, Bong Jik; Han, Jin Hee; Park, Hye‐Rim; Kim, Min Young; Kim, Ah Reum; Oh, Seung‐Ha; Park, Woong‐Yang; Oh, Doo Yi; Lee, Seungmin; Choi, Byung Yoon Journal: Journal of gene medicine Issue: Volume 20:Number 6(2018) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. A haploid HSV‐1 genome platform for vector development: testing of the tetracycline‐responsive switch shows interference by infected cell protein 0. (October 2016) Authors: Khalique, Hena; López Marco, Jorge; Lim, Filip Journal: Journal of gene medicine Issue: Volume 18:Number 10(2016:Oct.) Page Start: 302 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. A homozygous missense variant in the homeobox domain of the NKX6‐2 results in progressive spastic ataxia type 8 associated with lower limb weakness and neurological manifestations. (16th April 2020) Authors: Almatrafi, Ahmad; Umair, Muhammad; Eldardear, Amr; Al‐Luqmani, Majid; Hashmi, Jamil A.; Albalawi, Alia M.; Alfadhel, Majid; Ramzan, Khushnooda; Basit, Sulman Journal: Journal of gene medicine Issue: Volume 22:Number 8(2020) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. A kidney injury molecule‐1 (Kim‐1) gene reporter in a mouse artificial chromosome: the responsiveness to cisplatin toxicity in immortalized mouse kidney S3 cells. (October 2016) Authors: Kokura, Kenji; Kuromi, Yasushi; Endo, Takeshi; Anzai, Naohiko; Kazuki, Yasuhiro; Oshimura, Mitsuo; Ohbayashi, Tetsuya Journal: Journal of gene medicine Issue: Volume 18:Number 10(2016:Oct.) Page Start: 273 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. A new NOTCH3 damaging variant in a thrombocytopenia family of Miao ethnic group. (22nd November 2019) Authors: Zhao, Yingling; Li, Juheng Journal: Journal of gene medicine Issue: Volume 21:Number 11(2019) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. A novel compound heterozygous variant linked to hematuria in a family with hereditary factor VII deficiency. (30th December 2021) Authors: Hu, Ya‐Nan; Gan, Yu‐Mian; Zhang, Yan‐Ping; Ruan, Dan‐Dan; Zhu, Yao‐Bin; Lin, Xin‐Fu; Fang, Zhu‐Ting; Liao, Li‐Sheng; Tang, Fa‐Qiang; Luo, Jie‐Wei Journal: Journal of gene medicine Issue: Volume 24:Number 2(2022) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. A novel missense mutation in the UBE2A gene causes intellectual disability in the large X‐linked family. (7th January 2021) Authors: Arslan Satılmış, Saide Betül; Kurt, Emin Emre; Akçay, Ebru Perim; Sazci, Ali; Ceylan, Ahmet Cevdet Journal: Journal of gene medicine Issue: Volume 23:Number 2(2021) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. A novel mutation (c.1010G>T; p.R337L) in TP63 as a cause of split‐hand/foot malformation with hypodontia. (30th August 2019) Authors: Jin, Jie‐Yuan; Zeng, Lei; Li, Ke; He, Ji‐Qiang; Pang, Xiaoyang; Huang, Hao; Xiang, Rong; Tang, Ju‐Yu Journal: Journal of gene medicine Issue: Volume 21:Number 10(2019) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗