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Article

The 12q14 microdeletion syndrome: six new cases confirming the role of HMGA2 in growth

26 Jan 2011

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Identifiers

PMID: 21267005
DOI: 10.1038/ejhg.2010.215

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The 12q14 microdeletion syndrome: six new cases confirming the role of HMGA2 in growthPMID 21267005Read ↗

The 12q14 microdeletion syndrome: additional patients and further evidence that HMGA2 is an important genetic determinant for human height.Semantic proximity Read ↗

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Characterization of HMGA2 variants expands the spectrum of Silver-Russell syndrome.Semantic proximity Read ↗

A splicing mutation of the HMGA2 gene is associated with Silver-Russell syndrome phenotype.Semantic proximity Read ↗

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Deregulation of HMGA2 in an aggressive angiomyxoma with t(11;12)(q23;q15)Semantic proximity Read ↗

A common variant of HMGA2 is associated with adult and childhood height in the general population.Semantic proximity Read ↗

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