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Spread of X-chromosome inactivation into chromosome 15 is associated with Prader–Willi syndrome phenotype in a boy with a t(X;15)(p21.1;q11.2) translocation

Chromosome 15CytogeneticsGenetic DisorderGeneticsPathologyChromosome BiologyMolecular GeneticsX-chromosome InactivationChromosomal RearrangementMedicineChromosome 9