Identification of a subtle t(16;19)(p13.3;p13.3) in an infant with multiple congenital abnormalities using a 12-colour multiplex FISH telomere assay, M-TEL

Jill Brown, Sharon W. Horsley, Christine Jung, Kaan Saracoglu, Bart Janssen, Michaela Brough, Markus Daschner, Bernd Beedgen, Guido Kerkhoffs, Roland Eils, Peter C. Harris, Anna Jauch, Lyndal Kearney

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