Disruption of Contactin 4 (CNTN4) Results in Developmental Delay and Other Features of 3p Deletion Syndrome

3p deletion syndrome is a rare contiguous-gene disorder involving the loss of the telomeric portion of the short arm of chromosome 3 and characterized by developmental delay, growth retardation, and dysmorphic features. All reported cases have involved, at a minimum, the deletion of chromosome 3 tel...

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Main Authors: Fernandez, Thomas, Morgan, Thomas, Davis, Nicole, Klin, Ami, Morris, Ashley, Farhi, Anita, Lifton, Richard P., State, Matthew W.
פורמט: Artigo
שפה:Inglês
יצא לאור: The American Society of Human Genetics 2004
נושאים:
Report
גישה מקוונת:https://ncbi.nlm.nih.gov/pmc/articles/PMC1182094/
https://ncbi.nlm.nih.gov/pubmed/15106122
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