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3D-FISH analysis reveals chromatid cohesion defect during interphase in Roberts syndrome
BACKGROUND: Roberts syndrome (RBS) is a rare autosomal recessive disorder mainly characterized by growth retardation, limb defects and craniofacial anomalies. Characteristic cytogenetic findings are “railroad track” appearance of chromatids and premature centromere separation in metaphase spreads. M...
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Main Authors: | , , , , , , , , , , , , |
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格式: | Artigo |
語言: | Inglês |
出版: |
BioMed Central
2014
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主題: | |
在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4197286/ https://ncbi.nlm.nih.gov/pubmed/25320640 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13039-014-0059-6 |
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