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Journal of the European Academy of Dermatology and Venereology : JEADV
|
October 22, 2017
Apremilast for the treatment of moderate-to-severe palmoplantar psoriasis: results from a double-blind, placebo-controlled, randomized study
R Bissonnette, R Haydey, L A Rosoph, et al.
American Journal of Medical Genetics. Part A
|
December 2, 2017
Incomplete penetrance, variable expressivity, or dosage insensitivity in four families with directly transmitted unbalanced chromosome abnormalities
Mark S Bateman, Morag N Collinson, David J Bunyan, et al.
European Journal of Human Genetics : EJHG
|
October 18, 2007
8p23.1 duplication syndrome; a novel genomic condition with unexpected complexity revealed by array CGH
John C K Barber, Viv K Maloney, Shuwen Huang, et al.
Neurology
|
February 17, 2022
Cognitive Outcome 1 Year After Mild Traumatic Brain Injury: Results From the TRACK-TBI Study
Andrea L C Schneider, J Russell Huie, W John Boscardin, et al.
Journal of Neurotrauma
|
October 27, 2020
Validity of the Brief Test of Adult Cognition by Telephone in Level 1 Trauma Center Patients Six Months Post-Traumatic Brain Injury: A TRACK-TBI Study
Lindsay D Nelson, Jason K Barber, Nancy R Temkin, et al.
American Journal of Medical Genetics. Part A
|
January 5, 2011
Further molecular and clinical delineation of the Wisconsin syndrome phenotype associated with interstitial 3q24q25 deletions
Marjolein H Willemsen, Nicole de Leeuw, Catherine Mercer, et al.
JNCI Cancer Spectrum
|
October 9, 2024
Posttreatment surveillance intensity and overall survival in prostate cancer survivors (AFT-30)
Ronald C Chen, Ramsankar Basak, Stacie Dusetzina, et al.
Journal of Neurosurgery
|
August 12, 2017
Timing of cranioplasty: a 10.75-year single-center analysis of 754 patients
Ryan P Morton, Isaac Josh Abecassis, Josiah F Hanson, et al.
Anticancer Research
|
May 17, 2002
Frequent LOH at hMLH1, a highly variable SNP in hMSH3, and negligible coding instability in ovarian cancer
Iordanis I Arzimanoglou, Lise Lotte Hansen, David Chong, et al.
Clinical Genetics
|
October 2, 2009
Copy number changes of the microcephalin 1 gene (MCPH1) in patients with autism spectrum disorders
H M Ozgen, E van Daalen, P F Bolton, et al.
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of 24
Search research articles
Search
Showing results (211-220 of 234) with videos related to
Sort By:
Page
of 24
Journal of the European Academy of Dermatology and Venereology : JEADV
|
October 22, 2017
Apremilast for the treatment of moderate-to-severe palmoplantar psoriasis: results from a double-blind, placebo-controlled, randomized study
R Bissonnette, R Haydey, L A Rosoph, et al.
American Journal of Medical Genetics. Part A
|
December 2, 2017
Incomplete penetrance, variable expressivity, or dosage insensitivity in four families with directly transmitted unbalanced chromosome abnormalities
Mark S Bateman, Morag N Collinson, David J Bunyan, et al.
European Journal of Human Genetics : EJHG
|
October 18, 2007
8p23.1 duplication syndrome; a novel genomic condition with unexpected complexity revealed by array CGH
John C K Barber, Viv K Maloney, Shuwen Huang, et al.
Neurology
|
February 17, 2022
Cognitive Outcome 1 Year After Mild Traumatic Brain Injury: Results From the TRACK-TBI Study
Andrea L C Schneider, J Russell Huie, W John Boscardin, et al.
Journal of Neurotrauma
|
October 27, 2020
Validity of the Brief Test of Adult Cognition by Telephone in Level 1 Trauma Center Patients Six Months Post-Traumatic Brain Injury: A TRACK-TBI Study
Lindsay D Nelson, Jason K Barber, Nancy R Temkin, et al.
American Journal of Medical Genetics. Part A
|
January 5, 2011
Further molecular and clinical delineation of the Wisconsin syndrome phenotype associated with interstitial 3q24q25 deletions
Marjolein H Willemsen, Nicole de Leeuw, Catherine Mercer, et al.
JNCI Cancer Spectrum
|
October 9, 2024
Posttreatment surveillance intensity and overall survival in prostate cancer survivors (AFT-30)
Ronald C Chen, Ramsankar Basak, Stacie Dusetzina, et al.
Journal of Neurosurgery
|
August 12, 2017
Timing of cranioplasty: a 10.75-year single-center analysis of 754 patients
Ryan P Morton, Isaac Josh Abecassis, Josiah F Hanson, et al.
Anticancer Research
|
May 17, 2002
Frequent LOH at hMLH1, a highly variable SNP in hMSH3, and negligible coding instability in ovarian cancer
Iordanis I Arzimanoglou, Lise Lotte Hansen, David Chong, et al.
Clinical Genetics
|
October 2, 2009
Copy number changes of the microcephalin 1 gene (MCPH1) in patients with autism spectrum disorders
H M Ozgen, E van Daalen, P F Bolton, et al.
Page
of 24