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: Kaur, Maninder, DeScipio, Cheryl, McCallum, Jennifer, Yaeger, Dinah, Devoto, Marcella, Jackson, Laird G., Spinner, Nancy B., Krantz, Ian D.
Formato: Artigo
Idioma:Inglês
Publicado: 2005
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Article
Acceso en liña: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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