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)

The SinGapore Incidental Finding (SGIF) study group

doi:10.1038/s41436-018-0142-1

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)

The SinGapore Incidental Finding (SGIF) study group

Singapore Health Services
National University Hospital
KK Women's and Children's Hospital
Duke-NUS Medical School
National Heart Centre Singapore
National Cancer Centre
Agency for Science, Technology and Research, Singapore
National University of Singapore
Singapore National Eye Center

Research output: Contribution to journal › Comment/debate

2 Scopus citations

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.

Original language	English
Pages (from-to)	1692
Number of pages	1
Journal	Genetics in Medicine
Volume	20
Issue number	12
DOIs	https://doi.org/10.1038/s41436-018-0142-1
State	Published - 01 12 2018
Externally published	Yes

Bibliographical note

Publisher Copyright:
© 2018, American College of Medical Genetics and Genomics.

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10.1038/s41436-018-0142-1

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@article{87b98f372cb643e793274c2326e471db,

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)",

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.",

author = "\{The SinGapore Incidental Finding (SGIF) study group\} and Yasmin Bylstra and Kuan, \{Jyn Ling\} and Lim, \{Weng Khong\} and Bhalshankar, \{Jaydutt Digambar\} and Teo, \{Jing Xian\} and Sonia Davila and Teh, \{Bin Tean\} and Steve Rozen and Tan, \{Ene Choo\} and Liew, \{Wendy Kein Meng\} and Yeo, \{Khung Keong\} and Patrick Tan and Saw, \{Seang Mei\} and Cheng, \{Ching Yu\} and Stuart Cook and Roger Foo and Jamuar, \{Saumya Shekhar\}",

note = "Publisher Copyright: {\textcopyright} 2018, American College of Medical Genetics and Genomics.",

year = "2018",

month = dec,

day = "1",

doi = "10.1038/s41436-018-0142-1",

language = "英语",

volume = "20",

pages = "1692",

journal = "Genetics in Medicine",

issn = "1098-3600",

publisher = "Elsevier B.V.",

number = "12",

}

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T1 - Correction to

T2 - 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)

AU - The SinGapore Incidental Finding (SGIF) study group

AU - Bylstra, Yasmin

AU - Kuan, Jyn Ling

AU - Lim, Weng Khong

AU - Bhalshankar, Jaydutt Digambar

AU - Teo, Jing Xian

AU - Davila, Sonia

AU - Teh, Bin Tean

AU - Rozen, Steve

AU - Tan, Ene Choo

AU - Liew, Wendy Kein Meng

AU - Yeo, Khung Keong

AU - Tan, Patrick

AU - Saw, Seang Mei

AU - Cheng, Ching Yu

AU - Cook, Stuart

AU - Foo, Roger

AU - Jamuar, Saumya Shekhar

PY - 2018/12/1

Y1 - 2018/12/1

N2 - 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.

AB - 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.

UR - https://www.scopus.com/pages/publications/85052288239

U2 - 10.1038/s41436-018-0142-1

DO - 10.1038/s41436-018-0142-1

M3 - 评论/辩论

C2 - 30089799

AN - SCOPUS:85052288239

SN - 1098-3600

VL - 20

SP - 1692

JO - Genetics in Medicine

JF - Genetics in Medicine

IS - 12

ER -

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)

Abstract

Bibliographical note

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