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Journal of Forensic Sciences|March 28, 2008
Sarcoidosis and mechanisms of unexpected deathRoger W Byard, Nicholas Manton, Michael Tsokos
Orbit (Amsterdam, Netherlands)|January 11, 2021
Paediatric fronto-orbital osteoblastoma: case reportDavid S Curragh, Nicholas Manton, James Slattery, et al.
American Journal of Medical Genetics. Part A|August 3, 2016
Recurrent chronic histiocytic intervillositis with intrauterine growth restriction, osteopenia, and fracturesApril Crawford, Lynette Moore, Gregory Bennett, et al.
Pediatric Blood & Cancer|May 30, 2006
Rituximab for lymphoproliferative disease prior to haematopoietic stem cell transplantation for X-linked severe combined immunodeficiencyToby N Trahair, Brynn Wainstein, Nicholas Manton, et al.
American Journal of Medical Genetics. Part A|April 23, 2015
Phenotypic variation of TTC19-deficient mitochondrial complex III deficiency: a case report and literature reviewDylan A Mordaunt, Alexandra Jolley, Shanti Balasubramaniam, et al.
Brain : a Journal of Neurology|December 27, 2021
Bi-allelic loss-of-function OBSCN variants predispose individuals to severe recurrent rhabdomyolysisMacarena Cabrera-Serrano, Laure Caccavelli, Marco Savarese, et al.
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