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Neuron
|
March 10, 2001
A genetic analysis of neural progenitor differentiation
D H Geschwind, J Ou, M C Easterday, et al.
Molecular Psychiatry
|
October 17, 1998
Evidence that the dopamine D4 receptor is a susceptibility gene in attention deficit hyperactivity disorder
S L Smalley, J N Bailey, C G Palmer, et al.
Radiology
|
September 18, 2008
Relationship between gene expression and enhancement in glioblastoma multiforme: exploratory DNA microarray analysis
Whitney B Pope, Jenny H Chen, Jun Dong, et al.
Oncogene
|
April 18, 2003
Identification of molecular subtypes of glioblastoma by gene expression profiling
Paul S Mischel, Ruty Shai, Tao Shi, et al.
BMC Medical Genetics
|
June 3, 2014
De Novo variants in the KMT2A (MLL) gene causing atypical Wiedemann-Steiner syndrome in two unrelated individuals identified by clinical exome sequencing
Samuel P Strom, Reymundo Lozano, Hane Lee, et al.
American Journal of Human Genetics
|
August 7, 2004
Attention deficit hyperactivity disorder: fine mapping supports linkage to 5p13, 6q12, 16p13, and 17p11
Matthew N Ogdie, Simon E Fisher, May Yang, et al.
The Journal of Trauma and Acute Care Surgery
|
March 25, 2017
Characterization of distinct coagulopathic phenotypes in injury: Pathway-specific drivers and implications for individualized treatment
S Ariane Christie, Lucy Z Kornblith, Benjamin M Howard, et al.
Developmental Genetics
|
December 8, 1998
Klinefelter's syndrome as a model of anomalous cerebral laterality: testing gene dosage in the X chromosome pseudoautosomal region using a DNA microarray
D H Geschwind, J Gregg, K Boone, et al.
The Journal of Trauma and Acute Care Surgery
|
August 8, 2014
The effects of alcohol on coagulation in trauma patients: interpreting thrombelastography with caution
Benjamin M Howard, Lucy Z Kornblith, Brittney J Redick, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
June 3, 2026
Frequency of ZFHX3-Mediated Spinocerebellar Ataxia 4 in a US Undiagnosed Ataxia Cohort
Annie Chen, Udbhav Avadhani, Kathie Ngo, et al.
Page
of 84
Search research articles
Search
Showing results (651-660 of 835) with videos related to
Sort By:
Page
of 84
Neuron
|
March 10, 2001
A genetic analysis of neural progenitor differentiation
D H Geschwind, J Ou, M C Easterday, et al.
Molecular Psychiatry
|
October 17, 1998
Evidence that the dopamine D4 receptor is a susceptibility gene in attention deficit hyperactivity disorder
S L Smalley, J N Bailey, C G Palmer, et al.
Radiology
|
September 18, 2008
Relationship between gene expression and enhancement in glioblastoma multiforme: exploratory DNA microarray analysis
Whitney B Pope, Jenny H Chen, Jun Dong, et al.
Oncogene
|
April 18, 2003
Identification of molecular subtypes of glioblastoma by gene expression profiling
Paul S Mischel, Ruty Shai, Tao Shi, et al.
BMC Medical Genetics
|
June 3, 2014
De Novo variants in the KMT2A (MLL) gene causing atypical Wiedemann-Steiner syndrome in two unrelated individuals identified by clinical exome sequencing
Samuel P Strom, Reymundo Lozano, Hane Lee, et al.
American Journal of Human Genetics
|
August 7, 2004
Attention deficit hyperactivity disorder: fine mapping supports linkage to 5p13, 6q12, 16p13, and 17p11
Matthew N Ogdie, Simon E Fisher, May Yang, et al.
The Journal of Trauma and Acute Care Surgery
|
March 25, 2017
Characterization of distinct coagulopathic phenotypes in injury: Pathway-specific drivers and implications for individualized treatment
S Ariane Christie, Lucy Z Kornblith, Benjamin M Howard, et al.
Developmental Genetics
|
December 8, 1998
Klinefelter's syndrome as a model of anomalous cerebral laterality: testing gene dosage in the X chromosome pseudoautosomal region using a DNA microarray
D H Geschwind, J Gregg, K Boone, et al.
The Journal of Trauma and Acute Care Surgery
|
August 8, 2014
The effects of alcohol on coagulation in trauma patients: interpreting thrombelastography with caution
Benjamin M Howard, Lucy Z Kornblith, Brittney J Redick, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
June 3, 2026
Frequency of ZFHX3-Mediated Spinocerebellar Ataxia 4 in a US Undiagnosed Ataxia Cohort
Annie Chen, Udbhav Avadhani, Kathie Ngo, et al.
Page
of 84