Publication | Open Access

Molecular characterization of an X(p21.2;q28) chromosomal inversion in a Duchenne muscular dystrophy patient with mental retardation reveals a novel long non-coding gene on Xq28

Molecular CharacterizationMendelian DisorderChromosomal InversionGenetic DisorderGeneticsFragile X SpectrumMolecular BiologyMolecular GeneticsDisease Gene IdentificationMental RetardationMedicine