@article{naudion:hal-01214017,
TITLE = {Fetal phenotypes in otopalatodigital spectrum disorders},
AUTHOR = {Naudion, S. and Moutton, S. and Coupry, I. and Sole, G. and Deforges, J. and Guerineau, E. and Hubert, C{\'e}dric and Deves, S. and Pilliod, J. and Rooryck, C. and Abel, C. and Le Breton, F. and Collardeau-Frachon, S. and Cordier, M. P. and Delezoide, A. L. and Goldenberg, A. and Loget, P. and Melki, J. and Odent, S. and Patrier, S. and Verloes, A. and Viot, G. and Blesson, S. and Bessi{\`e}res, B. and Lacombe, D. and Arveiler, B. and Goizet, C. and Fergelot, P.},
URL = {https://univ-rennes.hal.science/hal-01214017},
JOURNAL = {Clinical Genetics},
PUBLISHER = {Wiley},
VOLUME = {89},
NUMBER = {3},
PAGES = {371--377},
YEAR = {2016},
MONTH = Mar, DOI = {10.1111/cge.12679},
KEYWORDS = {MNS ; FMD ; FLNA ; Melnick-Needles ; OPD2 ; Otopalatodigital ; filamin A ; frontometaphyseal dysplasia},
HAL_ID = {hal-01214017},
HAL_VERSION = {v1},
}