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A new chromosome 17q21.31 microdeletion syndrome associat... | ResearchHub
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A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism
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Authors
David Koolen
22 more
David Koolen
•
Lisenka Vissers
20 more
•
Bert Vries
Published
August 13, 2006
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Journal
Nature Genetics
Topics
Biology
Phenotype
Chromosomal Inversion
Chromosome
Microdeletion Syndrome
Show all topics
DOI
10.1038/ng1853
