@article{parenti:hal-01478812,
TITLE = {Mutations in chromatin regulators functionally link Cornelia de Lange syndrome and clinically overlapping phenotypes},
AUTHOR = {Parenti, Ilaria and Teresa-Rodrigo, Mar{\'i}a E. and Pozojevic, Jelena and Ruiz Gil, Sara and Bader, Ingrid and Braunholz, Diana and Bramswig, Nuria C. and Gervasini, Cristina and Larizza, Lidia and Pfeiffer, Lutz and Ozkinay, Ferda and Ramos, Feliciano and Reiz, Benedikt and Rittinger, Olaf and Strom, Tim M. and Watrin, Erwan and Wieczorek, Dagmar and Wollnik, Bernd and Baquero-Montoya, Carolina and Pi{\'e},
Juan and Deardorff, Matthew A. and Wendt, Kerstin and Gillessen-Kaesbach, Gabriele and Kaiser, Frank J.},
URL = {https://univ-rennes.hal.science/hal-01478812},
JOURNAL = {Human Genetics},
PUBLISHER = {Springer Verlag},
VOLUME = {136},
NUMBER = {3},
PAGES = {307-320},
YEAR = {2017},
MONTH = Mar, DOI = {10.1007/s00439-017-1758-y},
HAL_ID = {hal-01478812},
HAL_VERSION = {v1},
}