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Alison Salt

Showing results (31-40 of 38) with videos related to

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European Journal of Human Genetics : EJHG|April 7, 2026
Variants in the CxxC domain of the epigenetic regulator KDM2B support its role in developmental eye anomaliesFabiola Ceroni, Linda M Reis, Fiona Watkins, et al.
BMJ Open|June 24, 2018
Community-based parent-delivered early detection and intervention programme for infants at high risk of cerebral palsy in a low-resource country (Learning through Everyday Activities with Parents (LEAP-CP): protocol for a randomised controlled trialKatherine A Benfer, Iona Novak, Catherine Morgan, et al.
American Journal of Medical Genetics. Part A|April 7, 2005
SOX2 anophthalmia syndromeNicola K Ragge, Birgit Lorenz, Adele Schneider, et al.
The Journal of Pediatrics|June 28, 2025
Implementation Fidelity of a Smartphone Application for Population-Based General Movement Assessment: The Early Moves StudyCaroline F Alexander, Sarah E Hall, Alison Salt, et al.
American Journal of Human Genetics|February 7, 2008
Mutations in BMP4 cause eye, brain, and digit developmental anomalies: overlap between the BMP4 and hedgehog signaling pathwaysPreeti Bakrania, Maria Efthymiou, Johannes C Klein, et al.
BMJ Open|April 10, 2021
Early Moves: a protocol for a population-based prospective cohort study to establish general movements as an early biomarker of cognitive impairment in infantsCatherine Elliott, Caroline Alexander, Alison Salt, et al.
American Journal of Human Genetics|April 23, 2005
Heterozygous mutations of OTX2 cause severe ocular malformationsNicola K Ragge, Alison G Brown, Charlotte M Poloschek, et al.
BMJ Open|April 20, 2026
Vision Intervention for Seeing Impaired Babies: Learning through Enrichment (VISIBLE) - protocol of a feasibility pilot randomised controlled trialAndrea Guzzetta, Ada Bancale, Anna Bedoshvili, et al.
Pageof 4

Showing results (31-40 of 38) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 38 results.
European Journal of Human Genetics : EJHG|April 7, 2026
Variants in the CxxC domain of the epigenetic regulator KDM2B support its role in developmental eye anomaliesFabiola Ceroni, Linda M Reis, Fiona Watkins, et al.
BMJ Open|June 24, 2018
Community-based parent-delivered early detection and intervention programme for infants at high risk of cerebral palsy in a low-resource country (Learning through Everyday Activities with Parents (LEAP-CP): protocol for a randomised controlled trialKatherine A Benfer, Iona Novak, Catherine Morgan, et al.
American Journal of Medical Genetics. Part A|April 7, 2005
SOX2 anophthalmia syndromeNicola K Ragge, Birgit Lorenz, Adele Schneider, et al.
The Journal of Pediatrics|June 28, 2025
Implementation Fidelity of a Smartphone Application for Population-Based General Movement Assessment: The Early Moves StudyCaroline F Alexander, Sarah E Hall, Alison Salt, et al.
American Journal of Human Genetics|February 7, 2008
Mutations in BMP4 cause eye, brain, and digit developmental anomalies: overlap between the BMP4 and hedgehog signaling pathwaysPreeti Bakrania, Maria Efthymiou, Johannes C Klein, et al.
BMJ Open|April 10, 2021
Early Moves: a protocol for a population-based prospective cohort study to establish general movements as an early biomarker of cognitive impairment in infantsCatherine Elliott, Caroline Alexander, Alison Salt, et al.
American Journal of Human Genetics|April 23, 2005
Heterozygous mutations of OTX2 cause severe ocular malformationsNicola K Ragge, Alison G Brown, Charlotte M Poloschek, et al.
BMJ Open|April 20, 2026
Vision Intervention for Seeing Impaired Babies: Learning through Enrichment (VISIBLE) - protocol of a feasibility pilot randomised controlled trialAndrea Guzzetta, Ada Bancale, Anna Bedoshvili, et al.
Pageof 4