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Placenta
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January 8, 2025
Priority Setting Partnership on Placental Pathology: Consensus recommendations for placental research
Mauritia 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 tumors
Raisa 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 tumours
Jessica 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 children
Owen 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 children
Owen 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 Therapy
Melissa 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 development
Veronica 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 function
Lin Lin, Pascal Philibert, Bruno Ferraz-de-Souza, et al.
Ebiomedicine
|
June 23, 2016
Intra-Tumor Genetic Heterogeneity in Wilms Tumor: Clonal Evolution and Clinical Implications
George 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 study
Cally J Tann, Margaret Nakakeeto, Barbara A Willey, et al.
Page
of 37
Search research articles
Search
Showing results (311-320 of 369) with videos related to
Sort By:
Page
of 37
Placenta
|
January 8, 2025
Priority Setting Partnership on Placental Pathology: Consensus recommendations for placental research
Mauritia 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 tumors
Raisa 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 tumours
Jessica 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 children
Owen 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 children
Owen 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 Therapy
Melissa 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 development
Veronica 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 function
Lin Lin, Pascal Philibert, Bruno Ferraz-de-Souza, et al.
Ebiomedicine
|
June 23, 2016
Intra-Tumor Genetic Heterogeneity in Wilms Tumor: Clonal Evolution and Clinical Implications
George 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 study
Cally J Tann, Margaret Nakakeeto, Barbara A Willey, et al.
Page
of 37