Growth, development, and phenotypic spectrum of individuals with deletions of 2q33.1 involving SATB2

Zarate, Y.A., Bosanko, K.A., Thomas, M.A. et al. (18 more authors) (2021) Growth, development, and phenotypic spectrum of individuals with deletions of 2q33.1 involving SATB2. Clinical Genetics, 99 (4). pp. 547-557. ISSN 0009-9163

Abstract

Metadata

Authors/Creators:
  • Zarate, Y.A.
  • Bosanko, K.A.
  • Thomas, M.A.
  • Miller, D.T.
  • Cusmano‐Ozog, K.
  • Martinez‐Monseny, A.
  • Curry, C.J.
  • Graham, J.M.
  • Velsher, L.
  • Bekheirnia, M.R.
  • Seidel, V.
  • Dedousis, D.
  • Mitchell, A.L.
  • DiMarino, A.M.
  • Riess, A.
  • Balasubramanian, M. ORCID logo https://orcid.org/0000-0003-1488-3695
  • Fish, J.L.
  • Caffrey, A.R.
  • Fleischer, N.
  • Pierson, T.M.
  • Lacro, R.V.
Copyright, Publisher and Additional Information: © 2020 John Wiley & Sons A/S. This is an author-produced version of a paper subsequently published in Clinical Genetics. Uploaded in accordance with the publisher's self-archiving policy.
Keywords: 2q33.1 deletion; facial recognition technology; genotype–phenotype correlation; glass syndrome; SATB2; SATB2-associated syndrome
Dates:
  • Accepted: 28 December 2020
  • Published (online): 13 January 2021
  • Published: 5 March 2021
Institution: The University of Sheffield
Academic Units: The University of Sheffield > Faculty of Medicine, Dentistry and Health (Sheffield)
Depositing User: Symplectic Sheffield
Date Deposited: 18 Jun 2021 11:57
Last Modified: 13 Jan 2022 01:42
Status: Published
Publisher: Wiley
Refereed: Yes
Identification Number: https://doi.org/10.1111/cge.13912

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