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Ruth Armstrong

Showing results (21-30 of 61) with videos related to

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Quarterly Journal of Experimental Psychology (2006)|March 14, 2013
Verbal description benefits for faces when description conditions are unknown a prioriTodd C Jones, Ruth Armstrong, Allanah Casey, et al.
American Journal of Medical Genetics. Part A|March 28, 2013
Mosaic deletion of the NF1 gene in a patient with cognitive disability and dysmorphic features but without diagnostic features of NF1Ana Lisa Taylor Tavares, Lionel Willatt, Ruth Armstrong, et al.
Public Health Research & Practice|December 9, 2020
Converging crises: public interest journalism, the pandemic and public healthMelissa A Sweet, Megan Williams, Ruth Armstrong, et al.
Clinical Dysmorphology|September 8, 2006
Interstitial deletion of the short arm of chromosome 2 in a mother and child, with facial dysmorphism and mild learning difficultiesRuth Armstrong, Ian Ellis, Catherine Kightley, et al.
International Journal for Equity in Health|November 22, 2025
The collection and integration of data on migrants in health information systems: evidence from IrelandDeepanjali Vishwakarma, Soorej Jose Puthoopparambil, Anne MacFarlane, et al.
Neurogenetics|January 8, 2017
Mosaicism for a pathogenic MFN2 mutation causes minimal clinical features of CMT2A in the parent of a severely affected childKatherine Schon, Olivera Spasic-Boskovic, Kim Brugger, et al.
The Journal of Clinical Endocrinology and Metabolism|August 31, 2024
Approach to the Paediatric Patient With Suspected Pheochromocytoma or Paraganglioma Versus NeuroblastomaA Emile J Hendriks, Charlotte Burns, Ben Fleming, et al.
European Journal of Medical Genetics|April 27, 2018
Extending the clinical and genetic spectrum of ARID2 related intellectual disability. A case series of 7 patientsGabriella Gazdagh, Moira Blyth, Ingrid Scurr, et al.
Rheumatology (Oxford, England)|November 22, 2025
A Child with CANDLE Syndrome Presenting as Seronegative Polyarthritis Following Early ChemotherapySamantha Cooray, Alexander Wilson, Emma-Louise Gerety, et al.
Genes|October 29, 2025
Familial <i>NSD1</i> Exon 3 Deletion Associated with Phenotypic and Epigenetic VariabilitySunwoo Liv Lee, Alison Foster, Dalit May, et al.
Pageof 7

Showing results (21-30 of 61) with videos related to

Sort By:
Pageof 7
Quarterly Journal of Experimental Psychology (2006)|March 14, 2013
Verbal description benefits for faces when description conditions are unknown a prioriTodd C Jones, Ruth Armstrong, Allanah Casey, et al.
American Journal of Medical Genetics. Part A|March 28, 2013
Mosaic deletion of the NF1 gene in a patient with cognitive disability and dysmorphic features but without diagnostic features of NF1Ana Lisa Taylor Tavares, Lionel Willatt, Ruth Armstrong, et al.
Public Health Research & Practice|December 9, 2020
Converging crises: public interest journalism, the pandemic and public healthMelissa A Sweet, Megan Williams, Ruth Armstrong, et al.
Clinical Dysmorphology|September 8, 2006
Interstitial deletion of the short arm of chromosome 2 in a mother and child, with facial dysmorphism and mild learning difficultiesRuth Armstrong, Ian Ellis, Catherine Kightley, et al.
International Journal for Equity in Health|November 22, 2025
The collection and integration of data on migrants in health information systems: evidence from IrelandDeepanjali Vishwakarma, Soorej Jose Puthoopparambil, Anne MacFarlane, et al.
Neurogenetics|January 8, 2017
Mosaicism for a pathogenic MFN2 mutation causes minimal clinical features of CMT2A in the parent of a severely affected childKatherine Schon, Olivera Spasic-Boskovic, Kim Brugger, et al.
The Journal of Clinical Endocrinology and Metabolism|August 31, 2024
Approach to the Paediatric Patient With Suspected Pheochromocytoma or Paraganglioma Versus NeuroblastomaA Emile J Hendriks, Charlotte Burns, Ben Fleming, et al.
European Journal of Medical Genetics|April 27, 2018
Extending the clinical and genetic spectrum of ARID2 related intellectual disability. A case series of 7 patientsGabriella Gazdagh, Moira Blyth, Ingrid Scurr, et al.
Rheumatology (Oxford, England)|November 22, 2025
A Child with CANDLE Syndrome Presenting as Seronegative Polyarthritis Following Early ChemotherapySamantha Cooray, Alexander Wilson, Emma-Louise Gerety, et al.
Genes|October 29, 2025
Familial <i>NSD1</i> Exon 3 Deletion Associated with Phenotypic and Epigenetic VariabilitySunwoo Liv Lee, Alison Foster, Dalit May, et al.
Pageof 7