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Showing results (511-520 of 571) with videos related to

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Annals of Palliative Medicine|November 12, 2023
Addressing concerns and uncertainties surrounding the application of palliative radiotherapy in cases with a 30-day expected mortalityInmaculada Navarro-Domenech, Tara Behroozian, Peter Hoskin, et al.
Nature Genetics|October 19, 2004
Loss-of-function mutations in LEMD3 result in osteopoikilosis, Buschke-Ollendorff syndrome and melorheostosisJan Hellemans, Olena Preobrazhenska, Andy Willaert, et al.
Human Genetics|July 8, 2026
Implementation of exome sequencing for rare undiagnosed diseases in LMICs: the G2MC rare diseases exome sequencing pilot projectYasas D Kolambage, Claudia Gonzaga-Jauregui, Guillermo Lay-Son, et al.
Annals of Surgery|January 8, 2015
Living Donor Liver Transplantation in Children: Surgical and Immunological Results in 250 Recipients at Université Catholique de LouvainMichael Gurevich, Vanessa Guy-Viterbo, Magdalena Janssen, et al.
Blood|October 17, 2014
The H3K27me3 demethylase UTX is a gender-specific tumor suppressor in T-cell acute lymphoblastic leukemiaJoni Van der Meulen, Viraj Sanghvi, Konstantinos Mavrakis, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|March 15, 2022
Luminescent Human iPSC-Derived Neurospheroids Enable Modeling of Neurotoxicity After Oxygen-glucose DeprivationElise Van Breedam, Aleksandra Nijak, Tamariche Buyle-Huybrecht, et al.
Journal of Medical Genetics|October 18, 2013
3q27.3 microdeletional syndrome: a recognisable clinical entity associating dysmorphic features, marfanoid habitus, intellectual disability and psychosis with mood disorderJulien Thevenon, Patrick Callier, Hélène Poquet, et al.
Genes, Chromosomes & Cancer|December 18, 2020
Recurrent chromosomal imbalances provide selective advantage to human embryonic stem cells under enhanced replicative stress conditionsLiselot M Mus, Stéphane Van Haver, Mina Popovic, et al.
Plos One|November 14, 2019
Fanconi-BRCA pathway mutations in childhood T-cell acute lymphoblastic leukemiaGayle P Pouliot, James Degar, Laura Hinze, et al.
Medrxiv : the Preprint Server for Health Sciences|June 9, 2023
A novel neurodevelopmental syndrome caused by loss-of-function of the Zinc Finger Homeobox 3 (ZFHX3) geneMaría Del Rocío Pérez Baca, Eva Z Jacobs, Lies Vantomme, et al.
Pageof 58

Showing results (511-520 of 571) with videos related to

Sort By:
Pageof 58
Annals of Palliative Medicine|November 12, 2023
Addressing concerns and uncertainties surrounding the application of palliative radiotherapy in cases with a 30-day expected mortalityInmaculada Navarro-Domenech, Tara Behroozian, Peter Hoskin, et al.
Nature Genetics|October 19, 2004
Loss-of-function mutations in LEMD3 result in osteopoikilosis, Buschke-Ollendorff syndrome and melorheostosisJan Hellemans, Olena Preobrazhenska, Andy Willaert, et al.
Human Genetics|July 8, 2026
Implementation of exome sequencing for rare undiagnosed diseases in LMICs: the G2MC rare diseases exome sequencing pilot projectYasas D Kolambage, Claudia Gonzaga-Jauregui, Guillermo Lay-Son, et al.
Annals of Surgery|January 8, 2015
Living Donor Liver Transplantation in Children: Surgical and Immunological Results in 250 Recipients at Université Catholique de LouvainMichael Gurevich, Vanessa Guy-Viterbo, Magdalena Janssen, et al.
Blood|October 17, 2014
The H3K27me3 demethylase UTX is a gender-specific tumor suppressor in T-cell acute lymphoblastic leukemiaJoni Van der Meulen, Viraj Sanghvi, Konstantinos Mavrakis, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|March 15, 2022
Luminescent Human iPSC-Derived Neurospheroids Enable Modeling of Neurotoxicity After Oxygen-glucose DeprivationElise Van Breedam, Aleksandra Nijak, Tamariche Buyle-Huybrecht, et al.
Journal of Medical Genetics|October 18, 2013
3q27.3 microdeletional syndrome: a recognisable clinical entity associating dysmorphic features, marfanoid habitus, intellectual disability and psychosis with mood disorderJulien Thevenon, Patrick Callier, Hélène Poquet, et al.
Genes, Chromosomes & Cancer|December 18, 2020
Recurrent chromosomal imbalances provide selective advantage to human embryonic stem cells under enhanced replicative stress conditionsLiselot M Mus, Stéphane Van Haver, Mina Popovic, et al.
Plos One|November 14, 2019
Fanconi-BRCA pathway mutations in childhood T-cell acute lymphoblastic leukemiaGayle P Pouliot, James Degar, Laura Hinze, et al.
Medrxiv : the Preprint Server for Health Sciences|June 9, 2023
A novel neurodevelopmental syndrome caused by loss-of-function of the Zinc Finger Homeobox 3 (ZFHX3) geneMaría Del Rocío Pérez Baca, Eva Z Jacobs, Lies Vantomme, et al.
Pageof 58