Phenotype and natural history in 49 individuals with SATB2- associated syndrome

Zarate, Y.A., Gambello, M., Pandya, A. et al. (19 more authors) (2018) Phenotype and natural history in 49 individuals with SATB2- associated syndrome. In: American Journal of Medical Genetics Part A. 38th Annual David W. Smith Workshop on Malformations and Morphogenesis, 26-29 Aug 2017, Stowe, VT. Wiley , pp. 1526-1527.

Metadata

Item Type: Proceedings Paper
Authors/Creators:

This paper has 22 authors. You can scroll the list below to see them all or them all.

  • Zarate, Y.A.
  • Gambello, M.
  • Pandya, A.
  • Saenz, M.
  • Siu, V.M.
  • Ray, J.
  • Sellars, E.
  • Sun, A.
  • Smith, W.
  • Robin, N.H.
  • Picker, J.
  • Kirby, A.
  • Slavotinek, A.
  • Bebin, M.
  • Calhoun, A.
  • Desai, S.
  • Cohen, J.
  • Smith-Hicks, C.
  • Fatemi, A.
  • Abbott, M.-A.
  • Powell, C.M.
  • Balasubramanian, M. ORCID logo https://orcid.org/0000-0003-1488-3695
Copyright, Publisher and Additional Information:

© 2018 Wiley Periodicals, Inc.
Dates:
  • Published: 30 May 2018
  • Published (online): 25 April 2018
Institution: The University of Sheffield
Academic Units: The University of Sheffield > Faculty of Medicine, Dentistry and Health (Sheffield) > Department of Oncology (Sheffield)
Depositing User: Symplectic Sheffield
Date Deposited: 23 Aug 2018 10:16
Last Modified: 23 Aug 2018 10:22
Published Version: https://doi.org/10.1002/ajmg.a.38698
Status: Published
Publisher: Wiley
Refereed: Yes
Identification Number: 10.1002/ajmg.a.38698
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Open Archives Initiative ID (OAI ID):

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