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International Journal of Audiology|January 16, 2008
Consanguinity and deafness in Omani childrenMazin Al Khabori, Michael A PattonClinical Dysmorphology|June 15, 2004
Oculoauriculovertebral spectrum phenotype caused by an unbalanced t(5;8)(p15.31;p23.1) rearrangementDragana J Josifova, Michael A Patton, Karen MarksClinical Dysmorphology|June 26, 2010
A family with hereditary congenital facial paresis and a brief review of the literatureIsmail S Alrashdi, Philip Rich, Michael A PattonThe Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|September 9, 2004
A suspected case of Abruzzo-Erickson syndromeGiles Kidner, James Taylor, Michael A Patton, et al.American Journal of Medical Genetics. Part A|October 17, 2006
Further phenotypic and genetic variation in ADULT syndromeTom T Reisler, Michael A Patton, Peter P J MeagherJournal of Neurology|September 17, 2004
Troyer syndrome revisited. A clinical and radiological study of a complicated hereditary spastic paraplegiaChristos Proukakis, Harold Cross, Heema Patel, et al.Human Genetics|August 1, 2007
Novel Robinow syndrome causing mutations in the proximal region of the frizzled-like domain of ROR2 are retained in the endoplasmic reticulumBassam R Ali, Steve Jeffery, Neha Patel, et al.Genomics|April 5, 2003
The identification of a conserved domain in both spartin and spastin, mutated in hereditary spastic paraplegiaFrancesca D Ciccarelli, Christos Proukakis, Heema Patel, et al.American Journal of Human Genetics|October 18, 2003
Maspardin is mutated in mast syndrome, a complicated form of hereditary spastic paraplegia associated with dementiaMichael A Simpson, Harold Cross, Christos Proukakis, et al.Pageof 4