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Robin Forbes

Showing results (11-20 of 27) with videos related to

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Journal of Medical Screening|March 30, 2006
Using record linkage and manual follow-up to evaluate the Victorian maternal serum screening quadruple test for Down's syndrome, trisomy 18 and neural tube defectsAlice M Jaques, Veronica R Collins, Kerry Haynes, et al.
Canadian Oncology Nursing Journal = Revue Canadienne De Nursing Oncologique|May 8, 2023
Suzanne Rowland, Robin Forbes, Doris Howell, et al.
Canadian Oncology Nursing Journal = Revue Canadienne De Nursing Oncologique|May 8, 2023
Psychosocial and supportive care needs of individuals with advanced myelomaSuzanne Rowland, Robin Forbes, Doris Howell, et al.
Genes|April 10, 2019
Clinical and Molecular Differences between 4-Year-Old Monozygous Male Twins Mosaic for Normal, Premutation and Fragile X Full Mutation AllelesAlison Pandelache, Emma K Baker, Solange M Aliaga, et al.
Neuromuscular Disorders : NMD|March 23, 2024
Rare homozygous disease-associated sequence variants in children with spinal muscular atrophy: a phenotypic description and review of the literatureLimin Li, Manoj P Menezes, Melanie Smith, et al.
Supportive Care in Cancer : Official Journal of the Multinational Association of Supportive Care in Cancer|January 23, 2026
Exploring the information needs of breast cancer patients and families in a large, urban, academic hospital: perceived barriers and facilitators to finding relevant and credible informationMohamed Ugas, Eleni Giannopoulos, Jessica Tan, et al.
Muscle & Nerve|April 15, 2022
Delivering multidisciplinary neuromuscular care for children via telehealthKate Carroll, Justine Adams, Katy de Valle, et al.
Journal of the Neurological Sciences|July 30, 2025
Detailed immune cell profiling of paediatric patient with limb girdle muscular dystrophy R3Chantal A Coles, Sedi Jalali, Katy de Valle, et al.
Stem Cell Research|June 22, 2021
Generating an iPSC line (with isogenic control) from the PBMCs of an ACTA1 (p.Gly148Asp) nemaline myopathy patientPeter J Houweling, Chantal A Coles, Chrystal F Tiong, et al.
Genetics in Medicine Open|December 23, 2024
Rapid genomic testing in critically ill pediatric patients: Genetic counseling lessons from a national programKirsten Boggs, Fiona Lynch, Michelle Ward, et al.
Pageof 3

Showing results (11-20 of 27) with videos related to

Sort By:
Pageof 3
Journal of Medical Screening|March 30, 2006
Using record linkage and manual follow-up to evaluate the Victorian maternal serum screening quadruple test for Down's syndrome, trisomy 18 and neural tube defectsAlice M Jaques, Veronica R Collins, Kerry Haynes, et al.
Canadian Oncology Nursing Journal = Revue Canadienne De Nursing Oncologique|May 8, 2023
Suzanne Rowland, Robin Forbes, Doris Howell, et al.
Canadian Oncology Nursing Journal = Revue Canadienne De Nursing Oncologique|May 8, 2023
Psychosocial and supportive care needs of individuals with advanced myelomaSuzanne Rowland, Robin Forbes, Doris Howell, et al.
Genes|April 10, 2019
Clinical and Molecular Differences between 4-Year-Old Monozygous Male Twins Mosaic for Normal, Premutation and Fragile X Full Mutation AllelesAlison Pandelache, Emma K Baker, Solange M Aliaga, et al.
Neuromuscular Disorders : NMD|March 23, 2024
Rare homozygous disease-associated sequence variants in children with spinal muscular atrophy: a phenotypic description and review of the literatureLimin Li, Manoj P Menezes, Melanie Smith, et al.
Supportive Care in Cancer : Official Journal of the Multinational Association of Supportive Care in Cancer|January 23, 2026
Exploring the information needs of breast cancer patients and families in a large, urban, academic hospital: perceived barriers and facilitators to finding relevant and credible informationMohamed Ugas, Eleni Giannopoulos, Jessica Tan, et al.
Muscle & Nerve|April 15, 2022
Delivering multidisciplinary neuromuscular care for children via telehealthKate Carroll, Justine Adams, Katy de Valle, et al.
Journal of the Neurological Sciences|July 30, 2025
Detailed immune cell profiling of paediatric patient with limb girdle muscular dystrophy R3Chantal A Coles, Sedi Jalali, Katy de Valle, et al.
Stem Cell Research|June 22, 2021
Generating an iPSC line (with isogenic control) from the PBMCs of an ACTA1 (p.Gly148Asp) nemaline myopathy patientPeter J Houweling, Chantal A Coles, Chrystal F Tiong, et al.
Genetics in Medicine Open|December 23, 2024
Rapid genomic testing in critically ill pediatric patients: Genetic counseling lessons from a national programKirsten Boggs, Fiona Lynch, Michelle Ward, et al.
Pageof 3