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

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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
figure1

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.

Reference

  1. 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.

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Author information

Correspondence to Juliana Dourado Grzesiuk.

Additional information

The online version of the original article can be found under doi:10.1186/s13039-016-0249-5.

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Grzesiuk, J.D., Pereira, C.S., Grangeiro, C.H.P. et al. Erratum to: Familial chromosomal translocation X; 22 associated with infertility and recurrent X mosaicism. Mol Cytogenet 9, 53 (2016) doi:10.1186/s13039-016-0262-8

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