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Clinical Dysmorphology|June 7, 2007
Osteogenesis imperfecta and holoprosencephalyHelen Wainwright, Peter BeightonClinical Dysmorphology|March 17, 2005
The facio-audio-symphalangism syndrome in a four generation family with a nonsense mutation in the NOG-geneJ J van den Ende, P Mattelaer, F Declau, et al.Clinical Dysmorphology|March 17, 2005
Tubular skin appendage, renal agenesis and popliteal web: a further example of the human homologue of disorganization (Ds)E Esra Önal, Canan Türkyilmaz, Yıldız Atalay, et al.Clinical Dysmorphology|March 17, 2005
Case report: Y;6 translocation with deletion of 6pOphir D Klein, Kendall Backstrand, Philip D Cotter, et al.Clinical Dysmorphology|October 18, 2003
Siblings with glaucoma, mental retardation and short statureAli AlKaissi, Aza Hammou, Maher Ben Ghachem, et al.Clinical Dysmorphology|October 18, 2003
Large interstitial deletion of chromosome 13q and severe short stature: clinical report and review of the literatureAnne M Slavotinek, Felicitas LacbawanClinical Dysmorphology|October 18, 2003
A large deletion (1.5 Mb) encompassing the neurofibromatosis type 1 (NF1) gene in a patient with sporadic NF1 associated with dysmorphism, mental retardation, and unusual ocular and skeletal featuresCagatay Oktenli, Mutlu Saglam, Seref Demirbas, et al.Clinical Dysmorphology|October 18, 2003
Fusion of vertebrae, diaphragmatic hernia and unusual facies in a girl: a possible further case of Mathieu syndromeLeopoldo Zelante, Maria M RuscittoClinical Dysmorphology|October 18, 2003
Osteofibrous dysplasia in a Japanese boy with Costello syndromeTomohiro Kamoda, Akira Matsui, Naoyuki OchiaiPageof 117