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Emma Williams

Showing results (11-20 of 117) with videos related to

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Clinical Chemistry|May 15, 2007
Selected exonic sequencing of the AGXT gene provides a genetic diagnosis in 50% of patients with primary hyperoxaluria type 1Emma Williams, Gill Rumsby
British Journal of Psychology (London, England : 1953)|May 29, 2002
Sharing humour and laughter in autism and Down's syndromeVasudevi Reddy, Emma Williams, Amy Vaughan
Pediatric Pulmonology|August 8, 2021
Carbon dioxide monitoring in the newborn infantEmma Williams, Theodore Dassios, Anne Greenough
Pediatric Pulmonology|March 19, 2020
Assessment of sidestream end-tidal capnography in ventilated infants on the neonatal unitEmma Williams, Theodore Dassios, Anne Greenough
Journal of Perinatal Medicine|September 3, 2020
Antenatal and perinatal outcomes of refugees in high income countriesSarah Sturrock, Emma Williams, Anne Greenough
British Journal of Nursing (Mark Allen Publishing)|December 15, 2022
Promoting academic resilience through peer support in a new pre-registration nursing programmeMark Edwards, Emma Williams, Kevin Akerman
International Journal of Language & Communication Disorders|December 30, 2016
A systematic scoping review of speech and language therapists' public health practice for early language developmentClare Smith, Emma Williams, Karen Bryan
Kidney International|August 26, 2004
Evaluation of mutation screening as a first line test for the diagnosis of the primary hyperoxaluriasGill Rumsby, Emma Williams, Marion Coulter-Mackie
Autism : the International Journal of Research and Practice|November 17, 2005
Parents' experiences of introducing everyday object use to their children with autismEmma Williams, Linda Kendell-Scott, Alan Costall
Micropublication Biology|June 15, 2026
Gene model for the ortholog of <i>GstO3</i> in <i>Drosophila dunni</i>Emma Williams, Pablo Chialvo, Clare Scott Chialvo
Pageof 12

Showing results (11-20 of 117) with videos related to

Sort By:
Pageof 12
Clinical Chemistry|May 15, 2007
Selected exonic sequencing of the AGXT gene provides a genetic diagnosis in 50% of patients with primary hyperoxaluria type 1Emma Williams, Gill Rumsby
British Journal of Psychology (London, England : 1953)|May 29, 2002
Sharing humour and laughter in autism and Down's syndromeVasudevi Reddy, Emma Williams, Amy Vaughan
Pediatric Pulmonology|August 8, 2021
Carbon dioxide monitoring in the newborn infantEmma Williams, Theodore Dassios, Anne Greenough
Pediatric Pulmonology|March 19, 2020
Assessment of sidestream end-tidal capnography in ventilated infants on the neonatal unitEmma Williams, Theodore Dassios, Anne Greenough
Journal of Perinatal Medicine|September 3, 2020
Antenatal and perinatal outcomes of refugees in high income countriesSarah Sturrock, Emma Williams, Anne Greenough
British Journal of Nursing (Mark Allen Publishing)|December 15, 2022
Promoting academic resilience through peer support in a new pre-registration nursing programmeMark Edwards, Emma Williams, Kevin Akerman
International Journal of Language & Communication Disorders|December 30, 2016
A systematic scoping review of speech and language therapists' public health practice for early language developmentClare Smith, Emma Williams, Karen Bryan
Kidney International|August 26, 2004
Evaluation of mutation screening as a first line test for the diagnosis of the primary hyperoxaluriasGill Rumsby, Emma Williams, Marion Coulter-Mackie
Autism : the International Journal of Research and Practice|November 17, 2005
Parents' experiences of introducing everyday object use to their children with autismEmma Williams, Linda Kendell-Scott, Alan Costall
Micropublication Biology|June 15, 2026
Gene model for the ortholog of <i>GstO3</i> in <i>Drosophila dunni</i>Emma Williams, Pablo Chialvo, Clare Scott Chialvo
Pageof 12