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Cri du Chat syndrome
The Cri du Chat syndrome (CdCS) is a genetic disease resulting from a deletion of variable size occurring on the short arm of chromosome 5 (5p-). The incidence ranges from 1:15,000 to 1:50,000 live-born infants. The main clinical features are a high-pitched monochromatic cry, microcephaly, broad nas...
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2006
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1574300/ https://ncbi.nlm.nih.gov/pubmed/16953888 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1750-1172-1-33 |
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