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PDF] Distinctive Phenotype in a Case of Ring Chromosome 22 with Features of 22q13.3 Deletion Syndrome | Semantic Scholar
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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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Molecular characterisation of a ring chromosome 22 in a patient with severe language delay: a contribution to the refinement of the subtelomeric 22q deletion syndrome | Journal of Medical Genetics
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Patients I-V, VII-IX and XI-XIV, who present ring chromosomes 3, 4, 10,... | Download Scientific Diagram
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