PMCCPMCCPMCC

Search tips
Search criteria 

Advanced

 
Logo of molcytogenBioMed CentralBiomed Central Web Sitesearchsubmit a manuscriptregisterthis articleMolecular CytogeneticsJournal Front Page
 
Mol Cytogenet. 2016; 9: 53.
Published online 2016 July 5. doi:  10.1186/s13039-016-0262-8
PMCID: PMC4932718

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

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 ...

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.

Footnotes

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

Reference

1. Grzesiuk JD, Pereira CS, Grangeiro CHP, Picanço-Albuquerque CG, Oliveira-Gennaro FG, Machado FB, Medina-Acosta E, Ramos ES, Yoshimoto M, 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. [PMC free article] [PubMed] [Cross Ref]

Articles from Molecular Cytogenetics are provided here courtesy of BioMed Central