Search research articles
Contact Us
Filters
Showing results (41-50 of 186) with videos related to
Page
of 19
Sort By:
Human Mutation
|
January 17, 2002
Characterization of mutations in fifty North American patients with X-linked myotubular myopathy
Gail E Herman, Kevin Kopacz, Wei Zhao, et al.
Case Reports in Genetics
|
March 19, 2014
Mandibuloacral Dysplasia Caused by LMNA Mutations and Uniparental Disomy
Shaochun Bai, Anthony Lozada, Marilyn C Jones, et al.
European Journal of Human Genetics : EJHG
|
December 4, 2008
Intragenic deletions and duplications of the LIS1 and DCX genes: a major disease-causing mechanism in lissencephaly and subcortical band heterotopia
Eden V Haverfield, Amanda J Whited, Kristin S Petras, et al.
Archives of Virology
|
April 29, 2024
Development of an effective single-chain variable fragment recognizing a novel epitope in the hepatitis C virus E2 protein that restricts virus entry into hepatocytes
Soma Das, Padmanava Behera, Dipeshwari J Shewale, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
April 17, 2003
Progressive dystonia in a 12-year-old boy
Jörg Klepper, Jörg Schaper, Gordana Raca, et al.
European Journal of Inorganic Chemistry
|
February 6, 2014
Water-Soluble Derivatives of Octanuclear Iron-Oxo-Pyrazolato Complexes; An Experimental and Computational Study
Soma Das, Indranil Chakraborty, Dmitry Skachkov, et al.
Toxicological Sciences : an Official Journal of the Society of Toxicology
|
October 7, 2006
Structure-toxicity analysis of type-2 alkenes: in vitro neurotoxicity
Richard M Lopachin, David S Barber, Brian C Geohagen, et al.
European Journal of Human Genetics : EJHG
|
August 27, 2015
Reinitiation of mRNA translation in a patient with X-linked infantile spasms with a protein-truncating variant in ARX
Ching Moey, Scott Topper, Mary Karn, et al.
Brain & Development
|
June 4, 2013
The first case of CDK5RAP2-related primary microcephaly in a non-consanguineous patient identified by next generation sequencing
Christopher A Tan, Scott Topper, Catherine Ward Melver, et al.
Nucleic Acids Research
|
December 19, 2003
THGS: a web-based database of Transmembrane Helices in Genome Sequences
S A Fernando, P Selvarani, Soma Das, et al.
Page
of 19
Search research articles
Search
Showing results (41-50 of 186) with videos related to
Sort By:
Page
of 19
Human Mutation
|
January 17, 2002
Characterization of mutations in fifty North American patients with X-linked myotubular myopathy
Gail E Herman, Kevin Kopacz, Wei Zhao, et al.
Case Reports in Genetics
|
March 19, 2014
Mandibuloacral Dysplasia Caused by LMNA Mutations and Uniparental Disomy
Shaochun Bai, Anthony Lozada, Marilyn C Jones, et al.
European Journal of Human Genetics : EJHG
|
December 4, 2008
Intragenic deletions and duplications of the LIS1 and DCX genes: a major disease-causing mechanism in lissencephaly and subcortical band heterotopia
Eden V Haverfield, Amanda J Whited, Kristin S Petras, et al.
Archives of Virology
|
April 29, 2024
Development of an effective single-chain variable fragment recognizing a novel epitope in the hepatitis C virus E2 protein that restricts virus entry into hepatocytes
Soma Das, Padmanava Behera, Dipeshwari J Shewale, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
April 17, 2003
Progressive dystonia in a 12-year-old boy
Jörg Klepper, Jörg Schaper, Gordana Raca, et al.
European Journal of Inorganic Chemistry
|
February 6, 2014
Water-Soluble Derivatives of Octanuclear Iron-Oxo-Pyrazolato Complexes; An Experimental and Computational Study
Soma Das, Indranil Chakraborty, Dmitry Skachkov, et al.
Toxicological Sciences : an Official Journal of the Society of Toxicology
|
October 7, 2006
Structure-toxicity analysis of type-2 alkenes: in vitro neurotoxicity
Richard M Lopachin, David S Barber, Brian C Geohagen, et al.
European Journal of Human Genetics : EJHG
|
August 27, 2015
Reinitiation of mRNA translation in a patient with X-linked infantile spasms with a protein-truncating variant in ARX
Ching Moey, Scott Topper, Mary Karn, et al.
Brain & Development
|
June 4, 2013
The first case of CDK5RAP2-related primary microcephaly in a non-consanguineous patient identified by next generation sequencing
Christopher A Tan, Scott Topper, Catherine Ward Melver, et al.
Nucleic Acids Research
|
December 19, 2003
THGS: a web-based database of Transmembrane Helices in Genome Sequences
S A Fernando, P Selvarani, Soma Das, et al.
Page
of 19