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Iucrj
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January 23, 2018
Resolution extension by image summing in serial femtosecond crystallography of two-dimensional membrane-protein crystals
Cecilia M Casadei, Ching-Ju Tsai, Anton Barty, et al.
BMC Health Services Research
|
December 13, 2018
Standardized outcome measures for pregnancy and childbirth, an ICHOM proposal
Malini Anand Nijagal, Stephanie Wissig, Caleb Stowell, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences
|
June 11, 2014
7 Å resolution in protein two-dimensional-crystal X-ray diffraction at Linac Coherent Light Source
Bill Pedrini, Ching-Ju Tsai, Guido Capitani, et al.
Iucrj
|
July 31, 2014
Femtosecond X-ray diffraction from two-dimensional protein crystals
Matthias Frank, David B Carlson, Mark S Hunter, et al.
Neurology
|
April 30, 2020
Severe childhood speech disorder: Gene discovery highlights transcriptional dysregulation
Michael S Hildebrand, Victoria E Jackson, Thomas S Scerri, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 1, 2019
Recessive variants in ZNF142 cause a complex neurodevelopmental disorder with intellectual disability, speech impairment, seizures, and dystonia
Kamal Khan, Michael Zech, Angela T Morgan, et al.
Transfusion
|
February 9, 2020
Variations in hemoglobin measurement and eligibility criteria across blood donation services are associated with differing low-hemoglobin deferral rates: a BEST Collaborative study
Saurabh Zalpuri, Bas Romeijn, Elias Allara, et al.
Brain : a Journal of Neurology
|
January 13, 2022
Genome-wide association study of febrile seizures implicates fever response and neuronal excitability genes
Line Skotte, João Fadista, Jonas Bybjerg-Grauholm, et al.
Medrxiv : the Preprint Server for Health Sciences
|
December 3, 2025
Deep tissue sequencing improves genetic diagnostic yield in focal cortical dysplasia
Breana Galea, Joshua Reid, Samuel Gooley, et al.
American Journal of Human Genetics
|
October 15, 2020
Germline and Mosaic Variants in PRKACA and PRKACB Cause a Multiple Congenital Malformation Syndrome
Adrian Palencia-Campos, Phillip C Aoto, Erik M F Machal, et al.
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Search research articles
Search
Showing results (31-40 of 41) with videos related to
Sort By:
Page
of 5
Iucrj
|
January 23, 2018
Resolution extension by image summing in serial femtosecond crystallography of two-dimensional membrane-protein crystals
Cecilia M Casadei, Ching-Ju Tsai, Anton Barty, et al.
BMC Health Services Research
|
December 13, 2018
Standardized outcome measures for pregnancy and childbirth, an ICHOM proposal
Malini Anand Nijagal, Stephanie Wissig, Caleb Stowell, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences
|
June 11, 2014
7 Å resolution in protein two-dimensional-crystal X-ray diffraction at Linac Coherent Light Source
Bill Pedrini, Ching-Ju Tsai, Guido Capitani, et al.
Iucrj
|
July 31, 2014
Femtosecond X-ray diffraction from two-dimensional protein crystals
Matthias Frank, David B Carlson, Mark S Hunter, et al.
Neurology
|
April 30, 2020
Severe childhood speech disorder: Gene discovery highlights transcriptional dysregulation
Michael S Hildebrand, Victoria E Jackson, Thomas S Scerri, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 1, 2019
Recessive variants in ZNF142 cause a complex neurodevelopmental disorder with intellectual disability, speech impairment, seizures, and dystonia
Kamal Khan, Michael Zech, Angela T Morgan, et al.
Transfusion
|
February 9, 2020
Variations in hemoglobin measurement and eligibility criteria across blood donation services are associated with differing low-hemoglobin deferral rates: a BEST Collaborative study
Saurabh Zalpuri, Bas Romeijn, Elias Allara, et al.
Brain : a Journal of Neurology
|
January 13, 2022
Genome-wide association study of febrile seizures implicates fever response and neuronal excitability genes
Line Skotte, João Fadista, Jonas Bybjerg-Grauholm, et al.
Medrxiv : the Preprint Server for Health Sciences
|
December 3, 2025
Deep tissue sequencing improves genetic diagnostic yield in focal cortical dysplasia
Breana Galea, Joshua Reid, Samuel Gooley, et al.
American Journal of Human Genetics
|
October 15, 2020
Germline and Mosaic Variants in PRKACA and PRKACB Cause a Multiple Congenital Malformation Syndrome
Adrian Palencia-Campos, Phillip C Aoto, Erik M F Machal, et al.
Page
of 5