Open Access

Erratum to: Familial chromosomal translocation X; 22 associated with infertility and recurrent X mosaicism

  • Juliana Dourado Grzesiuk1Email author,
  • Ciro Silveira Pereira2,
  • Carlos Henrique Paiva Grangeiro1,
  • Clarissa Gondim Picanço-Albuquerque1,
  • Flávia Gaona Oliveira-Gennaro1,
  • Filipe Brum Machado3,
  • Enrique Medina-Acosta3,
  • Ester Silveira Ramos1,
  • Maisa Yoshimoto4 and
  • Lucia Martelli1
Molecular Cytogenetics20169:53

https://doi.org/10.1186/s13039-016-0262-8

Published: 5 July 2016

The original article was published in Molecular Cytogenetics 2016 9:45

Erratum

Unfortunately, the original version of this article [1] contained an error. Figure 2a was missing.
Fig. 2

FISH and Cytogenetic analyses of the translocation cariers. a FISH technique from patient A2 showing the subtelomeric probe of chromosome 22 (in green) in the distal portion of the short arm of the translocated X chromosome, while probe for TUPLE1 gene is located at band q11.21 (in red), remaining on the der(22). b On the left side the ideograms from normal chromosomes X and 22 show the breakpoints (red arrow) and the translocated segments (shaded in red). On the right side are the schematic ideograms and the GTG banding pattern of the derivative chromosomes

The correct version of Fig. 2a,b can be found below. Figure 2 has been corrected in the original article [1] and is also included correctly below.

Notes

Declarations

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Authors’ Affiliations

(1)
Genetics Department, Ribeirão Preto Medical School, University of Sao Paulo
(2)
Center of Biotecnology and Cellular Therapy, San Raphael Hospital
(3)
Center of Biosciences and Biotechnology, Darcy Ribeiro State University of Northern of Rio de Janeiro
(4)
Department of Medical Genetics, Faculty of Medical and Dentistry, University of Alberta

Reference

  1. Grzesiuk JD, Pereira CS, Grangeiro CHP, Picanço-Albuquerque CG, Oliveira-Gennaro FG, Machado FB, Medina-Acosta E, Ramos ES, Yoshimoto M and Martelli L. Familial chromosomal translocation X; 22 associated with infertility and recurrent X mosaicism. Mol Cytogenet. 2016;9:45. doi:10.1186/s13039-016-0249-5.View ArticlePubMedPubMed CentralGoogle Scholar

Copyright

© The Author(s). 2016

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