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A child with features of Goldenhar syndrome and a novel 1.12 Mb deletion in 22q11.2 by cytogenetics and oligonucleotide array CGH: Is this a candidate region for the syndrome?

Mendelian DisorderGenetic DisorderGeneticsPathogenesisPediatricsPathologyMb DeletionMolecular GeneticsDisease Gene IdentificationGoldenhar SyndromeMedicineOligonucleotide Array CghClinical Genetics