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)

10.1038/s41436-018-0142-1

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Bibliographic Details
Main 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
Other Authors: SAW SWEE HOCK SCHOOL OF PUBLIC HEALTH
Format: Article
Published: Nature Publishing Group 2019
Online Access:http://scholarbank.nus.edu.sg/handle/10635/152050
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Institution: National University of Singapore
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spelling sg-nus-scholar.10635-1520502024-04-17T09:33:24Z 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) 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 SAW SWEE HOCK SCHOOL OF PUBLIC HEALTH DUKE-NUS MEDICAL SCHOOL MEDICINE 10.1038/s41436-018-0142-1 Genetics in Medicine 2019-03-06T07:52:51Z 2019-03-06T07:52:51Z 2018 Article 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 10983600 http://scholarbank.nus.edu.sg/handle/10635/152050 Nature Publishing Group Scopus
institution National University of Singapore
building NUS Library
continent Asia
country Singapore
Singapore
content_provider NUS Library
collection ScholarBank@NUS
description 10.1038/s41436-018-0142-1
author2 SAW SWEE HOCK SCHOOL OF PUBLIC HEALTH
author_facet SAW SWEE HOCK SCHOOL OF PUBLIC HEALTH
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
format Article
author 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
spellingShingle 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
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)
author_sort Bylstra Y.
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)
title_short 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)
title_full 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)
title_fullStr 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)
title_full_unstemmed 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)
title_sort 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)
publisher Nature Publishing Group
publishDate 2019
url http://scholarbank.nus.edu.sg/handle/10635/152050
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