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.
| Autor: | Coci, Emanuele G., Koehler, Udo, Liehr, Thomas, Stelzner, Armin, Fink, Christian, Langen, Hendrik, Riedel, Joachim |
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| Předmět: | |
| Zdroj: | Molecular Cytogenetics (17558166); 3/9/2021, Vol. 14 Issue 1, p1-1, 1p |
| Abstrakt: | An amendment to this paper has been published and can be accessed via the original article. [ABSTRACT FROM AUTHOR] |
| Databáze: | Complementary Index |
| Externí odkaz: |
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