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Journal of Child Neurology|July 11, 2007
FGFR3 mutations and medial temporal lobe dysgenesisPeter Kannu, Salim AftimosAmerican Journal of Medical Genetics. Part A|November 20, 2004
Familial lipomyelomeningocele: a further reportPeter Kannu, Christopher Furneaux, Salim AftimosClinical Orthopaedics and Related Research|March 29, 2011
Two novel COL2A1 mutations associated with a Legg-Calvé-Perthes disease-like presentationPeter Kannu, Melita Irving, Salim Aftimos, et al.American Journal of Medical Genetics. Part A|October 16, 2007
An unclassifiable short rib-polydactyly syndrome with acromesomelic hypomineralization and campomelia in siblingsPeter Kannu, Jeannette H McFarlane, Ravi Savarirayan, et al.American Journal of Medical Genetics. Part A|February 22, 2011
Another case of multiple juxtasutural hyperostoses, cervical exostoses, and fatty infiltration of myocardiumPeter Kannu, David Perry, Martin Rees, et al.American Journal of Medical Genetics. Part A|September 21, 2007
Metatropic dysplasia: clinical and radiographic findings in 11 patients demonstrating long-term natural historyPeter Kannu, Salim Aftimos, Val Mayne, et al.American Journal of Medical Genetics. Part A|May 13, 2005
Another case of interstitial del(12) involving the proposed cardio-facio-cutaneous candidate regionPaul A James, Paul Oei, Daniel Ng, et al.American Journal of Medical Genetics. Part A|August 15, 2006
Epiphyseal dysplasia and other skeletal anomalies in a patient with the 6p25 microdeletion syndromePeter Kannu, Paul Oei, Howard R Slater, et al.Clinical Dysmorphology|November 18, 2008
Fetal methotrexate/aminopterin syndrome in an adult: a likely case with ectodermal abnormalitiesSalim AftimosClinical Dysmorphology|June 3, 2005
Blepharocheilodontic syndrome or lagophthalmos: a child with overlapping featuresIngrid Winship, Salim AftimosPageof 13