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Erratum to: Familial chromosomal translocation X; 22 associated with infertility and recurrent X mosaicism
Molecular Cytogenetics volume 9, Article number: 53 (2016)
The Original Article was published on 15 June 2016
Erratum
Unfortunately, the original version of this article [1] contained an error. Figure 2a was missing.
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
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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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). https://doi.org/10.1186/s13039-016-0262-8
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DOI: https://doi.org/10.1186/s13039-016-0262-8