Showing results (21-30 of 290) with videos related to
Sort By:
Pageof 29
Pediatric Radiology|November 3, 1998
Presentation of six cases of Stüve-Wiedemann syndromeV Cormier-Daire, A Munnich, S Lyonnet, et al.Journal of Medical Genetics|September 1, 1996
Clinical and genetic heterogeneity of hypochondroplasiaF Rousseau, J Bonaventure, L Legeai-Mallet, et al.Clinical Dysmorphology|July 12, 2001
A novel syndrome with dwarfism, poorly muscled build, absent clavicles, humeroradial fusion, slender bones, oligodactyly and micrognathiaL Faivre, V Cormier-Daire, D Geneviève, et al.Journal of Medical Genetics|October 1, 1992
The gene for hereditary multiple exostoses does not map to the Langer-Giedion region (8q23-q24)M Le Merrer, K Ben Othmane, V Stanescu, et al.Nature|September 15, 1994
Mutations in the gene encoding fibroblast growth factor receptor-3 in achondroplasiaF Rousseau, J Bonaventure, L Legeai-Mallet, et al.Hormone Research|January 1, 1996
Mutations of the fibroblast growth factor receptor-3 gene in achondroplasiaF Rousseau, J Bonaventure, L Legeai-Mallet, et al.Journal of Medical Genetics|October 1, 1994
OsteocraniostenosisA Verloes, F Narcy, B Grattagliano, et al.Journal of Medical Genetics|January 14, 2000
Exclusion of chromosome 9 helps to identify mild variants of acromesomelic dysplasia Maroteaux typeL Faivre, M Le Merrer, A Megarbane, et al.Human Genetics|March 1, 1997
An extension of the admixture test for the study of genetic heterogeneity in hereditary multiple exostosesL Legeai-Mallet, P Margaritte-Jeannin, M Lemdani, et al.Human Molecular Genetics|May 1, 1994
A gene for hereditary multiple exostoses maps to chromosome 19pM Le Merrer, L Legeai-Mallet, P M Jeannin, et al.Pageof 29