Showing results (261-270 of 290) with videos related to
Sort By:
Pageof 29
Journal of Pediatric Orthopedics. Part B|January 1, 1997
Acromesomelic dwarfism: a new variationF G Ferraz, P Maroteaux, J P Sousa, et al.Clinical Genetics|November 15, 2000
Linkage exclusion and mutational analysis of the noggin gene in patients with fibrodysplasia ossificans progressiva (FOP)M Q Xu, G Feldman, M Le Merrer, et al.Journal of Pediatric Orthopedics. Part B|January 1, 1997
Symmetrical enchondromatosis of the hands and feet in two sistersC R Mota, L Marques, E Silva, et al.Archives of Disease in Childhood|January 24, 2006
Wide clinical variability among 13 new Cockayne syndrome cases confirmed by biochemical assaysL Pasquier, V Laugel, L Lazaro, et al.Human Molecular Genetics|March 21, 1998
Clustering of mutations responsible for branchio-oto-renal (BOR) syndrome in the eyes absent homologous region (eyaHR) of EYA1S Abdelhak, V Kalatzis, R Heilig, et al.Clinical Genetics|December 1, 1996
Increased paternal age in CHARGE associationA L Tellier, S Lyonnet, V Cormier-Daire, et al.Journal De Genetique Humaine|January 1, 1985
[Osteodysplasia or the Melnick-Needles syndrome; (apropos of a new case)]B Deleporte, J P Buissart, P Vankemmel, et al.European Journal of Endocrinology|February 19, 2014
Unexpected high frequency of skeletal dysplasia in idiopathic short stature and small for gestational age patientsI Flechtner, K Lambot-Juhan, R Teissier, et al.Pediatric Radiology|February 7, 1998
Dyssegmental dysplasia: a case report of a Rolland-Desbuquois typeM C d'Orey, M Mateus, H Guimarães, et al.Clinical Dysmorphology|May 8, 1998
The cerebro-costo-mandibular syndrome: seven patients and review of the literatureJ J van den Ende, C Schrander-Stumpel, E Rupprecht, et al.Pageof 29