Published in
Oxford University Press, Human Molecular Genetics, p. ddw116, 2016
DOI: 10.1093/hmg/ddw116
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- Oxford University Press
- ORCID
- [www.ncbi.nlm.nih.gov] | PDF
- [www.researchgate.net]
- [europepmc.org] | PDF
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Systematic reanalysis of partial trisomy 21 cases with or without Down syndrome suggests a small region on 21q22.13 as critical to the phenotype
Journal article published in 2016 by
Maria Chiara Pelleri,
Elena Cicchini,
Chiara Locatelli,
Lorenza Vitale,
Maria Caracausi,
Allison Piovesan,
Alessandro Rocca 
,
Giulia Poletti,
Marco Seri,
Pierluigi Strippoli,
Guido Cocchi
,
Giulia Poletti,
Marco Seri,
Pierluigi Strippoli,
Guido Cocchi
This paper is made freely available by the publisher.
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