Patients with deletions of 9q22q34 do not define a syndrome: three case reports and a literature review

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Abstract
Three children with deletions involving the 9q22q34 region are described. A review of clinical features of these three new patients and seven previously reported ones did not demonstrate a recognizable dysmorphic pattern. Our cases illustrate the need for repeat karyotyping at higher levels of resolution when there is a suspicion of a chromosome anomaly, since each deletion was missed on initial analysis.