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Mutations in Cohesin Complex Members SMC3 and SMC1A Cause... | ResearchHub
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Mutations in Cohesin Complex Members SMC3 and SMC1A Cause a Mild Variant of Cornelia de Lange Syndrome with Predominant Mental Retardation
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Authors
Matthew Deardorff
17 more
Matthew Deardorff
•
Maninder Kaur
15 more
•
Jeffrey Milbrandt
Published
February 5, 2007
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Journal
The American Journal of Human Genetics
Topics
Biology
Molecular Biology
Genetics
Chromosome
Mutation
Show all topics
DOI
10.1086/511888
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publisher-specific-oa
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Journal
The American Journal of Human Genetics
Topics
Biology
Molecular Biology
Genetics
Chromosome
Mutation
Show all topics
DOI
10.1086/511888
License
publisher-specific-oa
