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. 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

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

2 Citations (Scopus)

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
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
Publication status	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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title = "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 = "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.

AU - Bainbridge, Matthew N.

AU - Yang, Yaping

AU - Liu, Pengfei

AU - Madan-Khetarpal, Suneeta

AU - Delgado, Mauricio R.

AU - Hudgins, Louanne

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

PY - 2020/4/1

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N2 - An amendment to this paper has been published and can be accessed via a link at the top of the paper.

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

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SN - 1098-3600

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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

ASJC Scopus subject areas

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