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Phenotypic correlations in a patient with ring chromosome 22

Ring chromosome 22, a rare cytogenetic anomaly, has been described in over 60 cases in the medical literature. The aim of this report was to present a case carrying ring chromosome 22, and her family. It is a case report of a patient presented at Medical Faculty of Çukurova University in Turkey. An...

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Detalhes bibliográficos
Main Authors: Demirhan, Osman, Tunç, Erdal
Formato: Artigo
Idioma:Inglês
Publicado em: Medknow Publications 2010
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2955959/
https://ncbi.nlm.nih.gov/pubmed/21031059
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0971-6866.69372
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