chromosomal translocation t(6;13)(q21;q12)

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Introduction

- chromosomal translocation t(6;13)(q21;q12) involving SNX3 may be a cause of microphthalmia syndromic type 8

More general terms

chromosomal translocation

References

↑ UniProt http://www.uniprot.org/uniprot/O60493.html

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