Correction: DYRK1A-related intellectual disability: a syndrome associated with congenital anomalies of the kidney and urinary tract (Genetics in Medicine, (2019), 21, 12, (2755-2764), 10.1038/s41436-019-0576-0)

Alexandria T.M. Blackburn; Nasim Bekheirnia; Vanessa C. Uma; Mark E. Corkins; Yuxiao Xu; Jill A. Rosenfeld; Matthew N. Bainbridge; Yaping Yang; Pengfei Liu; Suneeta Madan-Khetarpal; Mauricio R. Delgado; Louanne Hudgins; Ian Krantz; David Rodriguez-Buritica; Patricia G. Wheeler; Lihadh Al-Gazali; Aisha Mohamed Saeed Mohamed Al Shamsi; Natalia Gomez-Ospina; Hsiao Tuan Chao; Ghayda M. Mirzaa; Angela E. Scheuerle; Mary K. Kukolich; Fernando Scaglia; Christine Eng; Helen Rankin Willsey; Michael C. Braun; Dolores J. Lamb; Rachel K. Miller; Mir Reza Bekheirnia

doi:10.1038/s41436-019-0732-6

Correction: DYRK1A-related intellectual disability: a syndrome associated with congenital anomalies of the kidney and urinary tract (Genetics in Medicine, (2019), 21, 12, (2755-2764), 10.1038/s41436-019-0576-0)

Alexandria T.M. Blackburn, Nasim Bekheirnia, Vanessa C. Uma, Mark E. Corkins, Yuxiao Xu, Jill A. Rosenfeld, Matthew N. Bainbridge, Yaping Yang, Pengfei Liu, Suneeta Madan-Khetarpal, Mauricio R. Delgado, Louanne Hudgins, Ian Krantz, David Rodriguez-Buritica, Patricia G. Wheeler, Lihadh Al-Gazali, Aisha Mohamed Saeed Mohamed Al Shamsi, Natalia Gomez-Ospina, Hsiao Tuan Chao, Ghayda M. MirzaaAngela E. Scheuerle, Mary K. Kukolich, Fernando Scaglia, Christine Eng, Helen Rankin Willsey, Michael C. Braun, Dolores J. Lamb, Rachel K. Miller, Mir Reza Bekheirnia

Research output: Contribution to journal › Comment/debate › peer-review

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Abstract

An amendment to this paper has been published and can be accessed via a link at the top of the paper.

Original language	English (US)
Pages (from-to)	821
Number of pages	1
Journal	Genetics in Medicine
Volume	22
Issue number	4
DOIs	https://doi.org/10.1038/s41436-019-0732-6
State	Published - Apr 1 2020

ASJC Scopus subject areas

Genetics(clinical)

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Blackburn, A. T. M., Bekheirnia, N., Uma, V. C., Corkins, M. E., Xu, Y., Rosenfeld, J. A., Bainbridge, M. N., Yang, Y., Liu, P., Madan-Khetarpal, S., Delgado, M. R., Hudgins, L., Krantz, I., Rodriguez-Buritica, D., Wheeler, P. G., Al-Gazali, L., Shamsi, A. M. S. M. A., Gomez-Ospina, N., Chao, H. T., ... Bekheirnia, M. R. (2020). Correction: DYRK1A-related intellectual disability: a syndrome associated with congenital anomalies of the kidney and urinary tract (Genetics in Medicine, (2019), 21, 12, (2755-2764), 10.1038/s41436-019-0576-0). Genetics in Medicine, 22(4), 821. https://doi.org/10.1038/s41436-019-0732-6

Correction: DYRK1A-related intellectual disability: a syndrome associated with congenital anomalies of the kidney and urinary tract (Genetics in Medicine, (2019), 21, 12, (2755-2764), 10.1038/s41436-019-0576-0). / Blackburn, Alexandria T.M.; Bekheirnia, Nasim; Uma, Vanessa C. et al.
In: Genetics in Medicine, Vol. 22, No. 4, 01.04.2020, p. 821.

Research output: Contribution to journal › Comment/debate › peer-review

Blackburn, ATM, Bekheirnia, N, Uma, VC, Corkins, ME, Xu, Y, Rosenfeld, JA, Bainbridge, MN, Yang, Y, Liu, P, Madan-Khetarpal, S, Delgado, MR, Hudgins, L, Krantz, I, Rodriguez-Buritica, D, Wheeler, PG, Al-Gazali, L, Shamsi, AMSMA, Gomez-Ospina, N, Chao, HT, Mirzaa, GM, Scheuerle, AE, Kukolich, MK, Scaglia, F, Eng, C, Willsey, HR, Braun, MC, Lamb, DJ, Miller, RK & Bekheirnia, MR 2020, 'Correction: DYRK1A-related intellectual disability: a syndrome associated with congenital anomalies of the kidney and urinary tract (Genetics in Medicine, (2019), 21, 12, (2755-2764), 10.1038/s41436-019-0576-0)', Genetics in Medicine, vol. 22, no. 4, pp. 821. https://doi.org/10.1038/s41436-019-0732-6

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abstract = "An amendment to this paper has been published and can be accessed via a link at the top of the paper.",

author = "Blackburn, {Alexandria T.M.} and Nasim Bekheirnia and Uma, {Vanessa C.} and Corkins, {Mark E.} and Yuxiao Xu and Rosenfeld, {Jill A.} and Bainbridge, {Matthew N.} and Yaping Yang and Pengfei Liu and Suneeta Madan-Khetarpal and Delgado, {Mauricio R.} and Louanne Hudgins and Ian Krantz and David Rodriguez-Buritica and Wheeler, {Patricia G.} and Lihadh Al-Gazali and Shamsi, {Aisha Mohamed Saeed Mohamed Al} and Natalia Gomez-Ospina and Chao, {Hsiao Tuan} and Mirzaa, {Ghayda M.} and Scheuerle, {Angela E.} and Kukolich, {Mary K.} and Fernando Scaglia and Christine Eng and Willsey, {Helen Rankin} and Braun, {Michael C.} and Lamb, {Dolores J.} and Miller, {Rachel K.} and Bekheirnia, {Mir Reza}",

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AU - Blackburn, Alexandria T.M.

AU - Bekheirnia, Nasim

AU - Uma, Vanessa C.

AU - Corkins, Mark E.

AU - Xu, Yuxiao

AU - Rosenfeld, Jill A.

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AU - Liu, Pengfei

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AU - Krantz, Ian

AU - Rodriguez-Buritica, David

AU - Wheeler, Patricia G.

AU - Al-Gazali, Lihadh

AU - Shamsi, Aisha Mohamed Saeed Mohamed Al

AU - Gomez-Ospina, Natalia

AU - Chao, Hsiao Tuan

AU - Mirzaa, Ghayda M.

AU - Scheuerle, Angela E.

AU - Kukolich, Mary K.

AU - Scaglia, Fernando

AU - Eng, Christine

AU - Willsey, Helen Rankin

AU - Braun, Michael C.

AU - Lamb, Dolores J.

AU - Miller, Rachel K.

AU - Bekheirnia, Mir Reza

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Correction: DYRK1A-related intellectual disability: a syndrome associated with congenital anomalies of the kidney and urinary tract (Genetics in Medicine, (2019), 21, 12, (2755-2764), 10.1038/s41436-019-0576-0)

Abstract

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