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  • Erratum
  • Open Access

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

  • 1Email author,
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  • 1,
  • 3,
  • 3,
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  • 4 and
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Molecular Cytogenetics20169:53

  • Published:

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


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



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Authors’ Affiliations

Genetics Department, Ribeirão Preto Medical School, University of Sao Paulo, Ribeirao Preto, 14049-900, Brazil
Center of Biotecnology and Cellular Therapy, San Raphael Hospital, Salvador, 41253-190, Brazil
Center of Biosciences and Biotechnology, Darcy Ribeiro State University of Northern of Rio de Janeiro, Campos dos Goytacazes, 28013-600, Brazil
Department of Medical Genetics, Faculty of Medical and Dentistry, University of Alberta, Edmonton, Canada


  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


© The Author(s). 2016