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Precocious Sister Chromatid Separation (PSCS) in Cornelia de Lange Syndrome
The Cornelia de Lange syndrome (CdLS) (OMIM# 122470) is a dominantly inherited multisystem developmental disorder. The phenotype consists of characteristic facial features, hirsutism, abnormalities of the upper extremities ranging from subtle changes in the phalanges and metacarpal bones to oligodac...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2005
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2766539/ https://ncbi.nlm.nih.gov/pubmed/16100726 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.a.30919 |
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