Mapping of a Single Locus Capable of Complementing the Defective Heterochromatin Phenotype of Roberts Syndrome Cells

Roberts syndrome (RS) is a developmental disorder characterized by tetraphocomelia and a broad spectrum of additional clinical features. Most patients with RS exhibit characteristic cytogenetic phenotypes, which include an abnormal appearance of pericentromeric heterochromatin on metaphase chromosom...

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Bibliographische Detailangaben
Hauptverfasser: McDaniel, Lisa D. , Tomkins, Darrell J. , Stanbridge, Eric J. , Somerville, Martin J. , Friedberg, Errol C. , Schultz, Roger A. 
Format: Artigo
Sprache:Inglês
Veröffentlicht: American Society of Human Genetics 2005
Schlagworte:
Report
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC1226185/
https://ncbi.nlm.nih.gov/pubmed/15887093
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