4 Publications

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[4]
2020 | Journal Article | IST-REx-ID: 7488   OA
A. Latorre-Pellicer et al., “Evaluating Face2Gene as a tool to identify Cornelia de Lange syndrome by facial phenotypes,” International Journal of Molecular Sciences, vol. 21, no. 3, p. 1042, 2020.
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[3]
2020 | Journal Article | IST-REx-ID: 7957   OA
I. Parenti, L. E. Garcia Rabaneda, H. Schön, and G. Novarino, “Neurodevelopmental disorders: From genetics to functional pathways,” Trends in Neurosciences.
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[2]
2020 | Journal Article | IST-REx-ID: 7149
L. Avagliano et al., “Chromatinopathies: A focus on Cornelia de Lange syndrome,” Clinical Genetics, vol. 97, no. 1, pp. 3–11, 2020.
View | DOI | PubMed | Europe PMC
 
[1]
2020 | Journal Article | IST-REx-ID: 7877   OA
I. Parenti et al., “MAU2 and NIPBL variants impair the heterodimerization of the cohesin loader subunits and cause Cornelia de Lange syndrome,” Cell Reports, vol. 31, no. 7, p. 107647, 2020.
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4 Publications

Mark all

[4]
2020 | Journal Article | IST-REx-ID: 7488   OA
A. Latorre-Pellicer et al., “Evaluating Face2Gene as a tool to identify Cornelia de Lange syndrome by facial phenotypes,” International Journal of Molecular Sciences, vol. 21, no. 3, p. 1042, 2020.
View | Files available | DOI
 
[3]
2020 | Journal Article | IST-REx-ID: 7957   OA
I. Parenti, L. E. Garcia Rabaneda, H. Schön, and G. Novarino, “Neurodevelopmental disorders: From genetics to functional pathways,” Trends in Neurosciences.
View | DOI | Download (ext.)
 
[2]
2020 | Journal Article | IST-REx-ID: 7149
L. Avagliano et al., “Chromatinopathies: A focus on Cornelia de Lange syndrome,” Clinical Genetics, vol. 97, no. 1, pp. 3–11, 2020.
View | DOI | PubMed | Europe PMC
 
[1]
2020 | Journal Article | IST-REx-ID: 7877   OA
I. Parenti et al., “MAU2 and NIPBL variants impair the heterodimerization of the cohesin loader subunits and cause Cornelia de Lange syndrome,” Cell Reports, vol. 31, no. 7, p. 107647, 2020.
View | Files available | DOI
 

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Citation Style: IEEE

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