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Britta Hartmann

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

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European Journal of Medical Genetics|October 15, 2013
160 kb deletion in ISPD unmasking a recessive mutation in a patient with Walker-Warburg syndromeJohanna Christina Czeschik, Ute Hehr, Britta Hartmann, et al.
RNA (New York, N.Y.)|January 15, 2011
Distinct regulatory programs establish widespread sex-specific alternative splicing in Drosophila melanogasterBritta Hartmann, Robert Castelo, Belén Miñana, et al.
Orphanet Journal of Rare Diseases|October 22, 2014
Large homozygous RAB3GAP1 gene microdeletion causes Warburg micro syndrome 1Sylvie Picker-Minh, Andreas Busche, Britta Hartmann, et al.
Neuropediatrics|January 17, 2022
How to Detect Isolated PEX10-Related Cerebellar Ataxia?Esmeralda Nava, Britta Hartmann, Larissa Boxheimer, et al.
Case Reports in Hematology|June 8, 2026
Very Late Extramedullary Relapse of Acute Myeloid Leukemia 13 Years After Allogeneic Transplant: A Case ReportYvette von Aarburg, Astrid Beerlage, Darius Juskevicius, et al.
Endocrinology, Diabetes & Metabolism Case Reports|December 20, 2023
Barakat syndrome diagnosed decades after initial presentationUmberto Spennato, Jennifer Siegwart, Britta Hartmann, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 14, 2002
HOX genes in the sepiolid squid Euprymna scolopes: implications for the evolution of complex body plansPatrick Callaerts, Patricia N Lee, Britta Hartmann, et al.
Malaria Journal|September 1, 2023
Exploring the host factors affecting asymptomatic Plasmodium falciparum infection: insights from a rural Burkina Faso studyPeter J Neyer, Bérenger Kaboré, Christos T Nakas, et al.
The Journal of Allergy and Clinical Immunology|November 20, 2012
Clinical outcome in IL-10- and IL-10 receptor-deficient patients with or without hematopoietic stem cell transplantationKarin R Engelhardt, Neil Shah, Intan Faizura-Yeop, et al.
American Journal of Human Genetics|November 19, 2013
Loss-of-function mutations in TBC1D20 cause cataracts and male infertility in blind sterile mice and Warburg micro syndrome in humansRyan P Liegel, Mark T Handley, Adam Ronchetti, et al.
Pageof 2

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

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
European Journal of Medical Genetics|October 15, 2013
160 kb deletion in ISPD unmasking a recessive mutation in a patient with Walker-Warburg syndromeJohanna Christina Czeschik, Ute Hehr, Britta Hartmann, et al.
RNA (New York, N.Y.)|January 15, 2011
Distinct regulatory programs establish widespread sex-specific alternative splicing in Drosophila melanogasterBritta Hartmann, Robert Castelo, Belén Miñana, et al.
Orphanet Journal of Rare Diseases|October 22, 2014
Large homozygous RAB3GAP1 gene microdeletion causes Warburg micro syndrome 1Sylvie Picker-Minh, Andreas Busche, Britta Hartmann, et al.
Neuropediatrics|January 17, 2022
How to Detect Isolated PEX10-Related Cerebellar Ataxia?Esmeralda Nava, Britta Hartmann, Larissa Boxheimer, et al.
Case Reports in Hematology|June 8, 2026
Very Late Extramedullary Relapse of Acute Myeloid Leukemia 13 Years After Allogeneic Transplant: A Case ReportYvette von Aarburg, Astrid Beerlage, Darius Juskevicius, et al.
Endocrinology, Diabetes & Metabolism Case Reports|December 20, 2023
Barakat syndrome diagnosed decades after initial presentationUmberto Spennato, Jennifer Siegwart, Britta Hartmann, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 14, 2002
HOX genes in the sepiolid squid Euprymna scolopes: implications for the evolution of complex body plansPatrick Callaerts, Patricia N Lee, Britta Hartmann, et al.
Malaria Journal|September 1, 2023
Exploring the host factors affecting asymptomatic Plasmodium falciparum infection: insights from a rural Burkina Faso studyPeter J Neyer, Bérenger Kaboré, Christos T Nakas, et al.
The Journal of Allergy and Clinical Immunology|November 20, 2012
Clinical outcome in IL-10- and IL-10 receptor-deficient patients with or without hematopoietic stem cell transplantationKarin R Engelhardt, Neil Shah, Intan Faizura-Yeop, et al.
American Journal of Human Genetics|November 19, 2013
Loss-of-function mutations in TBC1D20 cause cataracts and male infertility in blind sterile mice and Warburg micro syndrome in humansRyan P Liegel, Mark T Handley, Adam Ronchetti, et al.
Pageof 2