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https://doi.org/10.1038/s41436-018-0142-1
Title: | Correction to: Population genomics in South East Asia captures unexpectedly high carrier frequency for treatable inherited disorders (Genetics in Medicine, (2018), 10.1038/s41436-018-0008-6) | Authors: | Bylstra Y. Kuan J.L. Lim W.K. Bhalshankar J.D. Teo J.X. Davila S. Teh B.T. Rozen S. Tan E.-C. Liew W.K.M. Yeo K.K. Tan P. Saw S.M. Cheng C.-Y. Cook S. Foo R. Jamuar S.S. The SinGapore Incidental Finding (SGIF) study group |
Issue Date: | 2018 | Publisher: | Nature Publishing Group | Citation: | Bylstra Y., Kuan J.L., Lim W.K., Bhalshankar J.D., Teo J.X., Davila S., Teh B.T., Rozen S., Tan E.-C., Liew W.K.M., Yeo K.K., Tan P., Saw S.M., Cheng C.-Y., Cook S., Foo R., Jamuar S.S., The SinGapore Incidental Finding (SGIF) study group (2018). Correction to: Population genomics in South East Asia captures unexpectedly high carrier frequency for treatable inherited disorders (Genetics in Medicine, (2018), 10.1038/s41436-018-0008-6). Genetics in Medicine. ScholarBank@NUS Repository. https://doi.org/10.1038/s41436-018-0142-1 | Abstract: | At the time of publication the author Jyn Ling Kuan did not have a master's degree; this has now been amended to BSc. This has now been corrected in the PDF and HTML versions of the article. © 2018, American College of Medical Genetics and Genomics. | Source Title: | Genetics in Medicine | URI: | http://scholarbank.nus.edu.sg/handle/10635/152050 | ISSN: | 10983600 | DOI: | 10.1038/s41436-018-0142-1 |
Appears in Collections: | Staff Publications Elements |
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