Add to ORKGAn international course for phycisians and scientistsThe 4th Annual Introductory Course on Skeletal Dysplasias, Freiburg, Germany, 5-9 July 2010
Campomelic dysplasia (CD) is a congenital disease causing skeletal defects, such as shortened and an...
Session: Anatomy - The Fate of the Chondrocyte in Development, Regeneration, and DiseaseMaintenance ...
Campomelic dysplasia (CD; OMIM #114290) is an autosomal dominant, frequently lethal dysplasia syndro...
abstractpublished_or_final_versionOrthopaedics and TraumatologyDoctoralDoctor of Philosoph
Symposium in Honor of Patrick Tam FRS "60 Years & Still Gastrulating"Conference Theme: From Embryolo...
Campomelic dysplasia (CD) is an autosomal, dominantly inherited, skeletal abnormality belonging to t...
Campomelic dysplasia (CD) is an autosomal, dominantly inherited, skeletal abnormality belonging to t...
Campomelic dysplasia (CD) is an autosomal, dominantly inherited, skeletal abnormality belonging to t...
An intensive six-week laboratory and lecture course for advanced graduate students, postdoctoral fel...
Human SOX9 mutations cause the skeletal malformation syndrome campomelic dysplasia (CD). Complete in...
Campomelic dysplasia is an alteration of bone development which is manifested as an autosomal domin...
Abstract OBJECTIVES: Campomelic dysplasia is a rare congenital skeletal disorder characterized by b...
It has previously been shown that, in the heterozygous state, mutations in the SOX9 gene cause campo...
Campomelic dysplasia is a skeletal dysplasia characterized by flat face, Pierre Robin sequence, shor...
Campomelic dysplasia (CD) is an autosomal dominant skeletal malformation syndrome with features incl...
Campomelic dysplasia (CD) is a congenital disease causing skeletal defects, such as shortened and an...
Session: Anatomy - The Fate of the Chondrocyte in Development, Regeneration, and DiseaseMaintenance ...
Campomelic dysplasia (CD; OMIM #114290) is an autosomal dominant, frequently lethal dysplasia syndro...
abstractpublished_or_final_versionOrthopaedics and TraumatologyDoctoralDoctor of Philosoph
Symposium in Honor of Patrick Tam FRS "60 Years & Still Gastrulating"Conference Theme: From Embryolo...
Campomelic dysplasia (CD) is an autosomal, dominantly inherited, skeletal abnormality belonging to t...
Campomelic dysplasia (CD) is an autosomal, dominantly inherited, skeletal abnormality belonging to t...
Campomelic dysplasia (CD) is an autosomal, dominantly inherited, skeletal abnormality belonging to t...
An intensive six-week laboratory and lecture course for advanced graduate students, postdoctoral fel...
Human SOX9 mutations cause the skeletal malformation syndrome campomelic dysplasia (CD). Complete in...
Campomelic dysplasia is an alteration of bone development which is manifested as an autosomal domin...
Abstract OBJECTIVES: Campomelic dysplasia is a rare congenital skeletal disorder characterized by b...
It has previously been shown that, in the heterozygous state, mutations in the SOX9 gene cause campo...
Campomelic dysplasia is a skeletal dysplasia characterized by flat face, Pierre Robin sequence, shor...
Campomelic dysplasia (CD) is an autosomal dominant skeletal malformation syndrome with features incl...
Campomelic dysplasia (CD) is a congenital disease causing skeletal defects, such as shortened and an...
Session: Anatomy - The Fate of the Chondrocyte in Development, Regeneration, and DiseaseMaintenance ...
Campomelic dysplasia (CD; OMIM #114290) is an autosomal dominant, frequently lethal dysplasia syndro...