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Simon Holden

Showing results (11-20 of 32) with videos related to

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Clinical Otolaryngology : Official Journal of ENT-UK ; Official Journal of Netherlands Society for Oto-Rhino-Laryngology & Cervico-Facial Surgery|May 27, 2026
Evaluation of the NHS R67 Monogenic Hearing Loss Panel in a Single UK CentreIrmak Sakin, Chloe Swords, Jessica Ball, et al.
European Journal of Human Genetics : EJHG|March 21, 2019
A case-note review of continued pregnancies found to be at a high risk of Huntington's disease: considerations for clinical practiceFelicity Wadrup, Simon Holden, Rhona MacLeod, et al.
Marine Biology|February 28, 2022
The ultrastructural development and 3D reconstruction of the transparent carapace of the ostracod <i>Skogsbergia lerneri</i>Benjamin M Rumney, F Tegwen Malik, Siân R Morgan, et al.
Thorax|June 19, 2021
Combining clinical, radiological and genetic approaches to pneumothorax managementHannah L Grimes, Simon Holden, Judith Babar, et al.
In Vitro Cellular & Developmental Biology. Animal|October 9, 2020
Establishment of long-term ostracod epidermal cultureSiân R Morgan, Laura Paletto, Benjamin Rumney, et al.
European Journal of Human Genetics : EJHG|February 25, 2026
Familial pneumothorax in twins with Tatton-Brown-Rahman DNMT3A overgrowth syndromeSarju G Mehta, Simon Holden, Judith Babar, et al.
American Journal of Medical Genetics. Part A|April 8, 2015
Clinical, structural, biochemical and X-ray crystallographic correlates of pathogenicity for variants in the C-propeptide region of the COL3A1 geneNatasha S Stembridge, Anthony M Vandersteen, Neeti Ghali, et al.
Journal of Medical Genetics|May 8, 2021
Genetic testing in motor neuron disease and frontotemporal dementia: a 5-year multicentre evaluationLauren M Cairns, Julia Rankin, Asma Hamad, et al.
Journal of Inherited Metabolic Disease|March 4, 2017
Mutations in SLC25A22: hyperprolinaemia, vacuolated fibroblasts and presentation with developmental delayEmma S Reid, Hywel Williams, Glenn Anderson, et al.
Journal of Medical Genetics|December 5, 2023
Short-read whole genome sequencing identifies causative variants in most individuals with previously unexplained aniridiaHildegard Nikki Hall, David Parry, Mihail Halachev, et al.
Pageof 4

Showing results (11-20 of 32) with videos related to

Sort By:
Pageof 4
Clinical Otolaryngology : Official Journal of ENT-UK ; Official Journal of Netherlands Society for Oto-Rhino-Laryngology & Cervico-Facial Surgery|May 27, 2026
Evaluation of the NHS R67 Monogenic Hearing Loss Panel in a Single UK CentreIrmak Sakin, Chloe Swords, Jessica Ball, et al.
European Journal of Human Genetics : EJHG|March 21, 2019
A case-note review of continued pregnancies found to be at a high risk of Huntington's disease: considerations for clinical practiceFelicity Wadrup, Simon Holden, Rhona MacLeod, et al.
Marine Biology|February 28, 2022
The ultrastructural development and 3D reconstruction of the transparent carapace of the ostracod <i>Skogsbergia lerneri</i>Benjamin M Rumney, F Tegwen Malik, Siân R Morgan, et al.
Thorax|June 19, 2021
Combining clinical, radiological and genetic approaches to pneumothorax managementHannah L Grimes, Simon Holden, Judith Babar, et al.
In Vitro Cellular & Developmental Biology. Animal|October 9, 2020
Establishment of long-term ostracod epidermal cultureSiân R Morgan, Laura Paletto, Benjamin Rumney, et al.
European Journal of Human Genetics : EJHG|February 25, 2026
Familial pneumothorax in twins with Tatton-Brown-Rahman DNMT3A overgrowth syndromeSarju G Mehta, Simon Holden, Judith Babar, et al.
American Journal of Medical Genetics. Part A|April 8, 2015
Clinical, structural, biochemical and X-ray crystallographic correlates of pathogenicity for variants in the C-propeptide region of the COL3A1 geneNatasha S Stembridge, Anthony M Vandersteen, Neeti Ghali, et al.
Journal of Medical Genetics|May 8, 2021
Genetic testing in motor neuron disease and frontotemporal dementia: a 5-year multicentre evaluationLauren M Cairns, Julia Rankin, Asma Hamad, et al.
Journal of Inherited Metabolic Disease|March 4, 2017
Mutations in SLC25A22: hyperprolinaemia, vacuolated fibroblasts and presentation with developmental delayEmma S Reid, Hywel Williams, Glenn Anderson, et al.
Journal of Medical Genetics|December 5, 2023
Short-read whole genome sequencing identifies causative variants in most individuals with previously unexplained aniridiaHildegard Nikki Hall, David Parry, Mihail Halachev, et al.
Pageof 4