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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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Frontiers | Ring Chromosome 20 Syndrome: Genetics, Clinical Characteristics, and Overlapping Phenotypes
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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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Complex biology of constitutional ring chromosomes structure and (in)stability revealed by somatic cell reprogramming | Scientific Reports
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