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Bishop, Nick, Adami, Silvano, Ahmed, S. Faisal, Anton, Jordi 
ORCID: 0000-0002-8792-4219, Arundel, Paul, Burren, Christine P., Devogelaer, Jean-Pierre, Hangartner, Thomas, Lane, Joseph M., Lorenc, Roman, Makitie, Outi ORCID: 0000-0002-4547-001X, Munns, Craig F., Paredes, Ana, Pavlov, Helene, Plotkin, Horacio, Raggio, Cathleen L., Loreto Reyes, Maria, Schoenau, Eckhard, Semler, Oliver ORCID: 0000-0003-0029-7556, Sillence, David O. and Steiner, Robert D. ORCID: 0000-0003-4177-4590
(2013).
Risedronate in children with osteogenesis imperfecta: a randomised, double-blind, placebo-controlled trial.
Lancet, 382 (9902).
S. 1424 - 1433.
NEW YORK:
ELSEVIER SCIENCE INC.
ISSN 1474-547X
Gordon, Christopher T., Xue, Shifeng ORCID: 0000-0002-4668-5952, Yigit, Goekhan, Filali, Hicham ORCID: 0000-0003-3352-740X, Chen, Kelan ORCID: 0000-0003-1973-5405, Rosins, Nadine, Yoshiura, Koh-ichiro, Oufadem, Myriam, Beck, Tamara J., McGowan, Ruth, Magee, Alex C., Altmueller, Janine, Dion, Camille, Thiele, Holger, Gurzau, Alexandra D., Nuernberg, Peter, Meschede, Dieter, Muehlbauer, Wolfgang, Okamoto, Nobuhiko, Varghese, Vinod, Irving, Rachel, Sigaudy, Sabine, Williams, Denise, Ahmed, S. Faisal, Bonnard, Carine, Kong, Mung Kei, Ratbi, Ilham, Fejjal, Nawfal, Fikri, Meriem, Elalaoui, Siham Chafai, Reigstad, Hallvard, Bole-Feysot, Christine, Nitschke, Patrick, Ragge, Nicola, Levy, Nicolas, Tuncbilek, Goekhan, Teo, Audrey S. M., Cunningham, Michael L., Sefiani, Abdelaziz, Kayserili, Huelya, Murphy, James M., Chatdokmaiprai, Chalermpong, Hillmer, Axel M., Wattanasirichaigoon, Duangrurdee, Lyonnet, Stanislas ORCID: 0000-0001-5426-9417, Magdinier, Frederique ORCID: 0000-0002-0159-9559, Javed, Asif, Blewitt, Marnie E., Amiel, Jeanne, Wollnik, Bernd and Reversade, Bruno
(2017).
De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal development.
Nature Genet., 49 (2).
S. 249 - 256.
NEW YORK:
NATURE PUBLISHING GROUP.
ISSN 1546-1718