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| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7941681 | PMC |
| http://dx.doi.org/10.1186/s13039-021-00534-5 | DOI Listing |
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Correction to: CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NFIA genes.
Mol Cytogenet
March 2021
Center of Social Pediatrics and Pediatric Neurology, General Hospital of Celle, 29221, Celle, Germany.
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