Clinical, cytogenetic and molecular analyses of a rare case with ring chromosome 15 and review of the literature
Objective: Ring chromosome 15 [r (15)], accompanied by a series of clinical symptoms, is a rare genetic disease. The genotype and phenotypic diversity of patients with r (15) still needed further enrichment. In this study we present a rare case of mosaic ring chromosome 15 with facial anomalies and...
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| Main Authors: | , , , , |
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| Format: | Book |
| Published: |
Elsevier,
2020-11-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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