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Plos One
|
March 8, 2011
Autism and increased paternal age related changes in global levels of gene expression regulation
Mark D Alter, Rutwik Kharkar, Keri E Ramsey, et al.
Plos One
|
July 16, 2015
A Frame-Shift Mutation in CAV1 Is Associated with a Severe Neonatal Progeroid and Lipodystrophy Syndrome
Isabelle Schrauwen, Szabolcs Szelinger, Ashley L Siniard, et al.
Journal of the National Cancer Institute
|
September 10, 2025
Challenges in the return of molecular tumor profiling results
Heinz-Josef Lenz, David W Craig, Kevin C Johnson, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
February 7, 2023
Impact of Genomic and Clinical Factors on Outcome of Children ≥18 Months of Age with Stage 3 Neuroblastoma with Unfavorable Histology and without MYCN Amplification: A Children's Oncology Group (COG) Report
Navin Pinto, Arlene Naranjo, Xiangming Ding, et al.
Brain : a Journal of Neurology
|
May 25, 2007
Polyhydramnios, megalencephaly and symptomatic epilepsy caused by a homozygous 7-kilobase deletion in LYK5
Erik G Puffenberger, Kevin A Strauss, Keri E Ramsey, et al.
Blood
|
April 25, 2012
Whole-genome sequencing of multiple myeloma from diagnosis to plasma cell leukemia reveals genomic initiating events, evolution, and clonal tides
Jan B Egan, Chang-Xin Shi, Waibhav Tembe, et al.
Investigative Ophthalmology & Visual Science
|
June 20, 2015
A De Novo Mutation in TEAD1 Causes Non-X-Linked Aicardi Syndrome
Isabelle Schrauwen, Szabolcs Szelinger, Ashley L Siniard, et al.
Human Molecular Genetics
|
May 2, 2007
Calmodulin-binding transcription activator 1 (CAMTA1) alleles predispose human episodic memory performance
Matthew J Huentelman, Andreas Papassotiropoulos, David W Craig, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)
|
October 8, 2008
Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies
Klaus-Peter Lesch, Nina Timmesfeld, Tobias J Renner, et al.
BMC Medical Genomics
|
June 20, 2014
Whole genome sequencing reveals potential targets for therapy in patients with refractory KRAS mutated metastatic colorectal cancer
Vijayalakshmi Shanmugam, Ramesh K Ramanathan, Nicole A Lavender, et al.
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of 17
Search research articles
Search
Showing results (71-80 of 161) with videos related to
Sort By:
Page
of 17
Plos One
|
March 8, 2011
Autism and increased paternal age related changes in global levels of gene expression regulation
Mark D Alter, Rutwik Kharkar, Keri E Ramsey, et al.
Plos One
|
July 16, 2015
A Frame-Shift Mutation in CAV1 Is Associated with a Severe Neonatal Progeroid and Lipodystrophy Syndrome
Isabelle Schrauwen, Szabolcs Szelinger, Ashley L Siniard, et al.
Journal of the National Cancer Institute
|
September 10, 2025
Challenges in the return of molecular tumor profiling results
Heinz-Josef Lenz, David W Craig, Kevin C Johnson, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
February 7, 2023
Impact of Genomic and Clinical Factors on Outcome of Children ≥18 Months of Age with Stage 3 Neuroblastoma with Unfavorable Histology and without MYCN Amplification: A Children's Oncology Group (COG) Report
Navin Pinto, Arlene Naranjo, Xiangming Ding, et al.
Brain : a Journal of Neurology
|
May 25, 2007
Polyhydramnios, megalencephaly and symptomatic epilepsy caused by a homozygous 7-kilobase deletion in LYK5
Erik G Puffenberger, Kevin A Strauss, Keri E Ramsey, et al.
Blood
|
April 25, 2012
Whole-genome sequencing of multiple myeloma from diagnosis to plasma cell leukemia reveals genomic initiating events, evolution, and clonal tides
Jan B Egan, Chang-Xin Shi, Waibhav Tembe, et al.
Investigative Ophthalmology & Visual Science
|
June 20, 2015
A De Novo Mutation in TEAD1 Causes Non-X-Linked Aicardi Syndrome
Isabelle Schrauwen, Szabolcs Szelinger, Ashley L Siniard, et al.
Human Molecular Genetics
|
May 2, 2007
Calmodulin-binding transcription activator 1 (CAMTA1) alleles predispose human episodic memory performance
Matthew J Huentelman, Andreas Papassotiropoulos, David W Craig, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)
|
October 8, 2008
Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies
Klaus-Peter Lesch, Nina Timmesfeld, Tobias J Renner, et al.
BMC Medical Genomics
|
June 20, 2014
Whole genome sequencing reveals potential targets for therapy in patients with refractory KRAS mutated metastatic colorectal cancer
Vijayalakshmi Shanmugam, Ramesh K Ramanathan, Nicole A Lavender, et al.
Page
of 17