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Article

Monozygotic twins with 17q21.31 microdeletion syndrome.

Twin research and human genetics : the official journal of the International Society for Twin Studies - 1 Oct 2014

Vlckova Marketa, Hancarova Miroslava, Drabova Jana, Slamova Zuzana, Koudova Monika, Alanova Renata, Mannik Katrin, Kurg Ants, Sedlacek Zdenek

Abstract excerpt

Chromosome 17q21.31 microdeletion syndrome is a genomic disorder caused by a recurrent 600 kb long deletion. The deletion affects the region of a common inversion present in about 20% of Europeans. The inversion is associated with the H2 haplotype carrying additional low-copy repeats susceptible to non-allelic homologous recombination, and this haplotype is prone to deletion. No instances of 17q21.31 deletions...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 24909117
DOI: 10.1017/thg.2014.29

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