P220: A de novo Xq13.2-13.3 duplication associated with non-syndromic intellectual disability by Grace Tan, Chun-Ping Liu, Poh-San Lai

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Embryo and fetal gene editing: Technical challenges and progress toward clinical applications by Citra N.Z. Mattar, Wei Leong Chew, Poh San Lai

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J’Accuse….. Or The Plight of pro-bono Volunteer Scientists in Academic Publishing by Juergen K. V. Reichardt, George P. Patrinos, Poh San Lai, Giuseppe Novelli

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P719: SMN1 deletion and silent carrier screening for spinal muscular atrophy by Poh San Lai, Grace Chia, Grace Tan, CP. Liu, PS. Low, Stacey Tay

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Mutation spectrum of RB1 mutations in retinoblastoma cases from Singapore with implications for genetic management and counselling. by Swati Tomar, Raman Sethi, Gangadhara Sundar, Thuan Chong Quah, Boon Long Quah, Poh San Lai

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Correction to: Association among dispositional mindfulness, self-compassion, and leukocyte telomere length in Chinese adults by Shian-Ling Keng, Onn Siong Yim, Poh San Lai, Soo Hong Chew, Richard P. Ebstein

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Dopaminergic polymorphisms associated with time-on-task declines and fatigue in the Psychomotor Vigilance Test. by Julian Lim, Richard Ebstein, Chun-Yu Tse, Mikhail Monakhov, Poh San Lai, David F Dinges, Kenneth Kwok

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Mutation spectrum analysis of DMD gene in Indonesian Duchenne and Becker muscular dystrophy patients [version 3; peer review: 2 approved] by Kristy Iskandar, Sunartini Hapsara, Chun Ping Liu, Rusdy Ghazali Malueka, Ery Kus Dwianingsih, . Gunadi, Masafumi Matsuo, Poh San Lai

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Dynamics of co-transcriptional pre-mRNA folding influences the induction of dystrophin exon skipping by antisense oligonucleotides. by Keng Boon Wee, Zacharias Aloysius Dwi Pramono, Jian Li Wang, Karl F MacDorman, Poh San Lai, Woon Chee Yee

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Genetics in Ischemic Stroke: Current Perspectives and Future Directions by Ka Zhang, Shaun S. E. Loong, Linus Z. H. Yuen, Narayanaswamy Venketasubramanian, Hui-Lin Chin, Poh San Lai, Benjamin Y. Q. Tan

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Germline genome modification through novel political, ethical, and social lenses. by Vicki Xafis, G Owen Schaefer, Markus K Labude, Yujia Zhu, Soren Holm, Roger Sik-Yin Foo, Poh San Lai, Ruth Chadwick

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Autosomal dominant Emery-Dreifuss muscular dystrophy caused by a mutation in the lamin A/C gene identified by exome sequencing: a case report by Kristy Iskandar, Sunartini, Farida Niken Astari, Rizki Amalia Gumilang, Nissya Ilma, Ni Putu Shartyanie, Guritno Adistyawan, Grace Tan, Gunadi, Poh San Lai

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Blending oxytocin and dopamine with everyday creativity by Anne Chong, Serenella Tolomeo, Yue Xiong, Dario Angeles, Mike Cheung, Benjamin Becker, Poh San Lai, Zhen Lei, Fabio Malavasi, Qianzi Tang, Soo Hong Chew, Richard P. Ebstein

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Effect of semaphorin 3C gene variants in multifactorial Hirschsprung disease by Gunadi, Fiko Ryantono, Raman Sethi, Marcellus, Alvin Santoso Kalim, Priscillia Imelda, Devy Melati, Susan Simanjaya, William Widitjiarso, Ririd Tri Pitaka, Nur Arfian, Kristy Iskandar, Akhmad Makhmudi, Poh San Lai

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The analysis of DMD gene deletions by multiplex PCR in Indonesian DMD/BMD patients: the era of personalized medicine by Kristy Iskandar, Ery Kus Dwianingsih, Linda Pratiwi, Alvin Santoso Kalim, Hasna Mardhiah, Alifiani H. Putranti, Dian K. Nurputra, Agung Triono, Elisabeth S. Herini, Rusdy G. Malueka, Gunadi, Poh San Lai, Sunartini

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