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American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|July 14, 2012
Ciliary disorder of the skeletonCeline Huber, Valerie Cormier-DaireEuropean Journal of Pediatrics|June 11, 2005
Severe, atypical form of dyschondrosteosis (report of two cases)Tadeusz Bieganski, Krzysztof Bik, Valerie Cormier-Daire, et al.American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|June 10, 2026
Review of the Molecular and Developmental Basis of Myhre Syndrome, Bench ResearchCamille Viaut, Valerie Cormier-DairePediatric Endocrinology Reviews : PER|April 28, 2009
Genetic and molecular aspects of acromelic dysplasiaCarine Le Goff, Valerie Cormier-DaireBonekey Reports|March 24, 2015
Chondrodysplasias and TGFβ signalingCarine Le Goff, Valerie Cormier-DaireBest Practice & Research. Clinical Endocrinology & Metabolism|March 15, 2011
The 3M syndromeCéline Huber, Arnold Munnich, Valerie Cormier-DairePediatric Blood & Cancer|October 10, 2013
Striking hematological abnormalities in patients with microcephalic osteodysplastic primordial dwarfism type II (MOPD II): a potential role of pericentrin in hematopoiesisSule Unal, Yasemin Alanay, Mualla Cetin, et al.Indian Pediatrics|May 10, 2016
Ghosal Type Hematodiaphyseal DysplasiaAmrit Jeevan, Mathilde Doyard, Madhulika Kabra, et al.Orphanet Journal of Rare Diseases|September 9, 2024
Osteogenesis Imperfecta: A study of the patient journey in 13 European countriesIngunn Westerheim, Valerie Cormier-Daire, Scott Gilbert, et al.European Journal of Medical Genetics|February 5, 2008
Novel mutation and atlantoaxial dislocation in two siblings from India with Dyggve-Melchior-Clausen syndromeK M Girisha, Valerie Cormier-Daire, Solange Heuertz, et al.Pageof 11