Correction: Population genomics in South East Asia captures unexpectedly high carrier frequency for treatable inherited disorders.
Publication
, Journal Article
Bylstra, Y; Kuan, JL; Lim, WK; Bhalshankar, JD; Teo, JX; Davila, S; Teh, BT; Rozen, S; Tan, E-C; Liew, WKM; Yeo, KK; Tan, P; Saw, SM; Foo, R ...
Published in: Genet Med
December 2018
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.
Duke Scholars
Published In
Genet Med
DOI
EISSN
1530-0366
Publication Date
December 2018
Volume
20
Issue
12
Start / End Page
1692
Location
United States
Related Subject Headings
- Genetics & Heredity
- 3105 Genetics
- 1103 Clinical Sciences
- 0604 Genetics
Citation
APA
Chicago
ICMJE
MLA
NLM
Bylstra, Y., Kuan, J. L., Lim, W. K., Bhalshankar, J. D., Teo, J. X., Davila, S., … Jamuar, S. S. (2018). Correction: Population genomics in South East Asia captures unexpectedly high carrier frequency for treatable inherited disorders. Genet Med, 20(12), 1692. https://doi.org/10.1038/s41436-018-0142-1
Bylstra, Yasmin, Jyn Ling Kuan, Weng Khong Lim, Jaydutt Digambar Bhalshankar, Jing Xian Teo, Sonia Davila, Bin Tean Teh, et al. “Correction: Population genomics in South East Asia captures unexpectedly high carrier frequency for treatable inherited disorders.” Genet Med 20, no. 12 (December 2018): 1692. https://doi.org/10.1038/s41436-018-0142-1.
Bylstra Y, Kuan JL, Lim WK, Bhalshankar JD, Teo JX, Davila S, et al. Correction: Population genomics in South East Asia captures unexpectedly high carrier frequency for treatable inherited disorders. Genet Med. 2018 Dec;20(12):1692.
Bylstra, Yasmin, et al. “Correction: Population genomics in South East Asia captures unexpectedly high carrier frequency for treatable inherited disorders.” Genet Med, vol. 20, no. 12, Dec. 2018, p. 1692. Pubmed, doi:10.1038/s41436-018-0142-1.
Bylstra Y, Kuan JL, Lim WK, Bhalshankar JD, Teo JX, Davila S, Teh BT, Rozen S, Tan E-C, Liew WKM, Yeo KK, Tan P, SinGapore Incidental Finding (SGIF) study group, Saw SM, Cheng C-Y, Cook S, Foo R, Jamuar SS. Correction: Population genomics in South East Asia captures unexpectedly high carrier frequency for treatable inherited disorders. Genet Med. 2018 Dec;20(12):1692.
Published In
Genet Med
DOI
EISSN
1530-0366
Publication Date
December 2018
Volume
20
Issue
12
Start / End Page
1692
Location
United States
Related Subject Headings
- Genetics & Heredity
- 3105 Genetics
- 1103 Clinical Sciences
- 0604 Genetics