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Genes | Free Full-Text | Prenatal Screening and Diagnostic Considerations for 22q11.2 Microdeletions
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Frontiers | Ring Chromosome 20 Syndrome: Genetics, Clinical Characteristics, and Overlapping Phenotypes
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Minute supernumerary ring chromosome 22 associated with cat eye syndrome: further delineation of the critical region. - Abstract - Europe PMC
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Clinical and cytogenetic analysis of terminal 22q13.3 deletion in two patients with ring chromosome 22 Ismail S, Kamel AK, Ashaat EA, Mohamed AM, Zaki MS, Aboul-Ezz EH, Hammad SA, Sayed IS, El
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