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Deirdre Devaney

Showing results (11-20 of 15) with videos related to

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Brain & Development|January 9, 2017
Symmetrical thalamic calcification: A trio whole exome sequencing negative seriesKathleen Mary Gorman, John James Aird, Judith Conroy, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|January 8, 2004
Parvovirus infects cardiac myocytes in hydrops fetalisAiveen O'Malley, Carole Barry-Kinsella, Caroline Hughes, et al.
Pediatric Nephrology (Berlin, Germany)|January 4, 2014
A rare cause of hypercalcemiaChia Wei Teoh, Irwin Gill, Rania Haydar, et al.
Journal of Clinical Microbiology|November 27, 2009
First report of sudden death due to myocarditis caused by adenovirus serotype 3Ann Treacy, Michael J Carr, Linda Dunford, et al.
Journal of Inherited Metabolic Disease|April 29, 2015
Clinical and genetic characterisation of infantile liver failure syndrome type 1, due to recessive mutations in LARSJillian P Casey, Suzanne Slattery, Melanie Cotter, et al.
Pageof 2

Showing results (11-20 of 15) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 15 results.
Brain & Development|January 9, 2017
Symmetrical thalamic calcification: A trio whole exome sequencing negative seriesKathleen Mary Gorman, John James Aird, Judith Conroy, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|January 8, 2004
Parvovirus infects cardiac myocytes in hydrops fetalisAiveen O'Malley, Carole Barry-Kinsella, Caroline Hughes, et al.
Pediatric Nephrology (Berlin, Germany)|January 4, 2014
A rare cause of hypercalcemiaChia Wei Teoh, Irwin Gill, Rania Haydar, et al.
Journal of Clinical Microbiology|November 27, 2009
First report of sudden death due to myocarditis caused by adenovirus serotype 3Ann Treacy, Michael J Carr, Linda Dunford, et al.
Journal of Inherited Metabolic Disease|April 29, 2015
Clinical and genetic characterisation of infantile liver failure syndrome type 1, due to recessive mutations in LARSJillian P Casey, Suzanne Slattery, Melanie Cotter, et al.
Pageof 2