Chromosome 17q21.31 duplication syndrome: Description of a new familiar case and further delineation of the clinical spectrum
文摘

First report of a familiar transmission of 17q21.31 duplication syndrome.

Description of the phenotype in proband and affected relatives.

Further delineation of the clinical spectrum.

Detailed description of neurobehavioral phenotype.

First evidence of complete penetrance with variable expressivity in affected relatives.

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