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Neil J Sebire

Showing results (311-320 of 369) with videos related to

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Placenta|January 8, 2025
Priority Setting Partnership on Placental Pathology: Consensus recommendations for placental researchMauritia C Marijnen, M I Bügel, T Yee Khong, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|December 3, 2008
Perilobar nephrogenic rests are nonobligate molecular genetic precursor lesions of insulin-like growth factor-II-associated Wilms tumorsRaisa Vuononvirta, Neil J Sebire, Anthony R Dallosso, et al.
Neuropathology and Applied Neurobiology|July 10, 2024
Decision making for health-related research outcomes that alter diagnosis: A model from paediatric brain tumoursJessica C Pickles, Kristian Aquilina, Jane Chalker, et al.
European Journal of Radiology|December 24, 2014
Diagnostic accuracy of post mortem MRI for abdominal abnormalities in foetuses and childrenOwen J Arthurs, Sudhin Thayyil, Catherine M Owens, et al.
European Radiology|September 1, 2014
Diagnostic accuracy of post-mortem MRI for thoracic abnormalities in fetuses and childrenOwen J Arthurs, Sudhin Thayyil, Oystein E Olsen, et al.
The Journal of Investigative Dermatology|June 11, 2021
Molecular Genetic Dissection of Inflammatory Linear Verrucous Epidermal Naevus Leads to Successful Targeted TherapyMelissa Riachi, Satyamaanasa Polubothu, Paulina Stadnik, et al.
The Journal of Investigative Dermatology|May 11, 2012
Germline melanocortin-1-receptor genotype is associated with severity of cutaneous phenotype in congenital melanocytic nevi: a role for MC1R in human fetal developmentVeronica A Kinsler, Sayeda Abu-Amero, Peter Budd, et al.
The Journal of Clinical Endocrinology and Metabolism|January 4, 2007
Heterozygous missense mutations in steroidogenic factor 1 (SF1/Ad4BP, NR5A1) are associated with 46,XY disorders of sex development with normal adrenal functionLin Lin, Pascal Philibert, Bruno Ferraz-de-Souza, et al.
Ebiomedicine|June 23, 2016
Intra-Tumor Genetic Heterogeneity in Wilms Tumor: Clonal Evolution and Clinical ImplicationsGeorge D Cresswell, John R Apps, Tasnim Chagtai, et al.
Archives of Disease in Childhood. Fetal and Neonatal Edition|August 7, 2017
Perinatal risk factors for neonatal encephalopathy: an unmatched case-control studyCally J Tann, Margaret Nakakeeto, Barbara A Willey, et al.
Pageof 37

Showing results (311-320 of 369) with videos related to

Sort By:
Pageof 37
Placenta|January 8, 2025
Priority Setting Partnership on Placental Pathology: Consensus recommendations for placental researchMauritia C Marijnen, M I Bügel, T Yee Khong, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|December 3, 2008
Perilobar nephrogenic rests are nonobligate molecular genetic precursor lesions of insulin-like growth factor-II-associated Wilms tumorsRaisa Vuononvirta, Neil J Sebire, Anthony R Dallosso, et al.
Neuropathology and Applied Neurobiology|July 10, 2024
Decision making for health-related research outcomes that alter diagnosis: A model from paediatric brain tumoursJessica C Pickles, Kristian Aquilina, Jane Chalker, et al.
European Journal of Radiology|December 24, 2014
Diagnostic accuracy of post mortem MRI for abdominal abnormalities in foetuses and childrenOwen J Arthurs, Sudhin Thayyil, Catherine M Owens, et al.
European Radiology|September 1, 2014
Diagnostic accuracy of post-mortem MRI for thoracic abnormalities in fetuses and childrenOwen J Arthurs, Sudhin Thayyil, Oystein E Olsen, et al.
The Journal of Investigative Dermatology|June 11, 2021
Molecular Genetic Dissection of Inflammatory Linear Verrucous Epidermal Naevus Leads to Successful Targeted TherapyMelissa Riachi, Satyamaanasa Polubothu, Paulina Stadnik, et al.
The Journal of Investigative Dermatology|May 11, 2012
Germline melanocortin-1-receptor genotype is associated with severity of cutaneous phenotype in congenital melanocytic nevi: a role for MC1R in human fetal developmentVeronica A Kinsler, Sayeda Abu-Amero, Peter Budd, et al.
The Journal of Clinical Endocrinology and Metabolism|January 4, 2007
Heterozygous missense mutations in steroidogenic factor 1 (SF1/Ad4BP, NR5A1) are associated with 46,XY disorders of sex development with normal adrenal functionLin Lin, Pascal Philibert, Bruno Ferraz-de-Souza, et al.
Ebiomedicine|June 23, 2016
Intra-Tumor Genetic Heterogeneity in Wilms Tumor: Clonal Evolution and Clinical ImplicationsGeorge D Cresswell, John R Apps, Tasnim Chagtai, et al.
Archives of Disease in Childhood. Fetal and Neonatal Edition|August 7, 2017
Perinatal risk factors for neonatal encephalopathy: an unmatched case-control studyCally J Tann, Margaret Nakakeeto, Barbara A Willey, et al.
Pageof 37