Search research articles
Contact Us
Filters
Showing results (151-160 of 174) with videos related to
Page
of 18
Sort By:
FEBS Open Bio
|
October 11, 2022
Molecular characterization of accripin11, a soluble shell protein with an acidic C-terminus, identified in the prismatic layer of the Mediterranean fan mussel Pinna nobilis (Bivalvia, Pteriomorphia)
Benazir Khurshid, Daniel J Jackson, Sylvain Engilberge, et al.
American Journal of Medical Genetics. Part A
|
November 1, 2018
Club foot in association with the 22q11.2 deletion syndrome: An observational study
Jelle F Homans, Terrence B Crowley, Erin Chen, et al.
American Journal of Medical Genetics. Part A
|
November 22, 2017
Orthopaedic manifestations within the 22q11.2 Deletion syndrome: A systematic review
Jelle F Homans, Isabel N Tromp, Dino Colo, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association
|
January 25, 2020
Defining Risk of Postoperative Obstructive Sleep Apnea in Patients With 22q11.2DS Undergoing Pharyngeal Flap Surgery for Velopharyngeal Dysfunction Using Polysomnographic Evaluation
Alfred Lee, Brian L Chang, Cynthia Solot, et al.
Chemical Reviews
|
June 6, 2014
Physicochemical properties of cells and their effects on intrinsically disordered proteins (IDPs)
Francois-Xavier Theillet, Andres Binolfi, Tamara Frembgen-Kesner, et al.
Physical Review. E, Statistical, Nonlinear, and Soft Matter Physics
|
May 18, 2013
Comparison between x-ray scattering and velocity-interferometry measurements from shocked liquid deuterium
K Falk, S P Regan, J Vorberger, et al.
Journal of Clinical Medicine
|
November 13, 2021
22q11.2 Deletion Syndrome as a Human Model for Idiopathic Scoliosis
Steven de Reuver, Jelle F Homans, Tom P C Schlösser, et al.
Archives of Disease in Childhood
|
April 9, 2018
Scoliosis in association with the 22q11.2 deletion syndrome: an observational study
Jelle F Homans, Vyaas G M Baldew, Rob C Brink, et al.
Scientific Reports
|
July 7, 2012
Testing quantum mechanics in non-Minkowski space-time with high power lasers and 4(th) generation light sources
B J B Crowley, R Bingham, R G Evans, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
December 4, 2018
Clinical validity assessment of genes frequently tested on hereditary breast and ovarian cancer susceptibility sequencing panels
Kristy Lee, Bryce A Seifert, Hermela Shimelis, et al.
Page
of 18
Search research articles
Search
Showing results (151-160 of 174) with videos related to
Sort By:
Page
of 18
FEBS Open Bio
|
October 11, 2022
Molecular characterization of accripin11, a soluble shell protein with an acidic C-terminus, identified in the prismatic layer of the Mediterranean fan mussel Pinna nobilis (Bivalvia, Pteriomorphia)
Benazir Khurshid, Daniel J Jackson, Sylvain Engilberge, et al.
American Journal of Medical Genetics. Part A
|
November 1, 2018
Club foot in association with the 22q11.2 deletion syndrome: An observational study
Jelle F Homans, Terrence B Crowley, Erin Chen, et al.
American Journal of Medical Genetics. Part A
|
November 22, 2017
Orthopaedic manifestations within the 22q11.2 Deletion syndrome: A systematic review
Jelle F Homans, Isabel N Tromp, Dino Colo, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association
|
January 25, 2020
Defining Risk of Postoperative Obstructive Sleep Apnea in Patients With 22q11.2DS Undergoing Pharyngeal Flap Surgery for Velopharyngeal Dysfunction Using Polysomnographic Evaluation
Alfred Lee, Brian L Chang, Cynthia Solot, et al.
Chemical Reviews
|
June 6, 2014
Physicochemical properties of cells and their effects on intrinsically disordered proteins (IDPs)
Francois-Xavier Theillet, Andres Binolfi, Tamara Frembgen-Kesner, et al.
Physical Review. E, Statistical, Nonlinear, and Soft Matter Physics
|
May 18, 2013
Comparison between x-ray scattering and velocity-interferometry measurements from shocked liquid deuterium
K Falk, S P Regan, J Vorberger, et al.
Journal of Clinical Medicine
|
November 13, 2021
22q11.2 Deletion Syndrome as a Human Model for Idiopathic Scoliosis
Steven de Reuver, Jelle F Homans, Tom P C Schlösser, et al.
Archives of Disease in Childhood
|
April 9, 2018
Scoliosis in association with the 22q11.2 deletion syndrome: an observational study
Jelle F Homans, Vyaas G M Baldew, Rob C Brink, et al.
Scientific Reports
|
July 7, 2012
Testing quantum mechanics in non-Minkowski space-time with high power lasers and 4(th) generation light sources
B J B Crowley, R Bingham, R G Evans, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
December 4, 2018
Clinical validity assessment of genes frequently tested on hereditary breast and ovarian cancer susceptibility sequencing panels
Kristy Lee, Bryce A Seifert, Hermela Shimelis, et al.
Page
of 18