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The presence of two rare genomic syndromes, 1q21 deletion and Xq28 duplication, segregating independently in a family with intellectual disability

Crossref DOI link: https://doi.org/10.1186/S13039-016-0286-0

Published Online: 2016-09-29

Published Print: 2016-12

Update policy: https://doi.org/10.1007/SPRINGER_CROSSMARK_POLICY

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