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A family with autism and rare copy number variants disrupting the Duchenne/Becker muscular dystrophy gene DMD and TRPM3.

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Academic year: 2021

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Figure

Fig. 1 Segregation of two rare CNVs in family 3019. a qPCR results for fine mapping distal and proximal ends of the DMD duplication.
Fig. 2 Further molecular characterisation of both rare CNVs. a Fibre FISH images from normal X chromosome from mother (upper) and duplicated X chromosome from proband (lower)

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