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Genomics
|
October 28, 2006
The DNA sequence of medaka chromosome LG22
Takashi Sasaki, Atsushi Shimizu, Sabine K Ishikawa, et al.
Zebrafish
|
April 2, 2008
Molecular analysis of the sex-determining region of the platyfish Xiphophorus maculatus
Christina Schultheis, Qingchun Zhou, Alexander Froschauer, et al.
Journal of Child Psychology and Psychiatry, and Allied Disciplines
|
February 23, 2017
SLC2A3 single-nucleotide polymorphism and duplication influence cognitive processing and population-specific risk for attention-deficit/hyperactivity disorder
Sören Merker, Andreas Reif, Georg C Ziegler, et al.
Genes
|
November 14, 2020
Genetic Spectrum of Syndromic and Non-Syndromic Hearing Loss in Pakistani Families
Julia Doll, Barbara Vona, Linda Schnapp, et al.
Cell
|
January 14, 2017
DNA Damage Signaling Instructs Polyploid Macrophage Fate in Granulomas
Laura Herrtwich, Indrajit Nanda, Konstantinos Evangelou, et al.
Cell
|
August 25, 2018
DNA Damage Signaling Instructs Polyploid Macrophage Fate in Granulomas
Laura Herrtwich, Indrajit Nanda, Konstantinos Evangelou, et al.
Medrxiv : the Preprint Server for Health Sciences
|
April 10, 2026
<i>FRMPD4</i> , a causal gene for intellectual disability and epilepsy, is associated with X-linked non-syndromic hearing loss
Daniel Liedtke, Kristen Rak, Katrina M Schrode, et al.
American Journal of Human Genetics
|
April 30, 2013
ZC4H2 mutations are associated with arthrogryposis multiplex congenita and intellectual disability through impairment of central and peripheral synaptic plasticity
Hiromi Hirata, Indrajit Nanda, Anne van Riesen, et al.
Cytogenetic and Genome Research
|
August 19, 2015
Third Report on Chicken Genes and Chromosomes 2015
Michael Schmid, Jacqueline Smith, David W Burt, et al.
Page
of 6
Search research articles
Search
Showing results (51-60 of 59) with videos related to
Sort By:
Page
of 6
You have reached the last page of results.
This site can display upto 59 results.
Genomics
|
October 28, 2006
The DNA sequence of medaka chromosome LG22
Takashi Sasaki, Atsushi Shimizu, Sabine K Ishikawa, et al.
Zebrafish
|
April 2, 2008
Molecular analysis of the sex-determining region of the platyfish Xiphophorus maculatus
Christina Schultheis, Qingchun Zhou, Alexander Froschauer, et al.
Journal of Child Psychology and Psychiatry, and Allied Disciplines
|
February 23, 2017
SLC2A3 single-nucleotide polymorphism and duplication influence cognitive processing and population-specific risk for attention-deficit/hyperactivity disorder
Sören Merker, Andreas Reif, Georg C Ziegler, et al.
Genes
|
November 14, 2020
Genetic Spectrum of Syndromic and Non-Syndromic Hearing Loss in Pakistani Families
Julia Doll, Barbara Vona, Linda Schnapp, et al.
Cell
|
January 14, 2017
DNA Damage Signaling Instructs Polyploid Macrophage Fate in Granulomas
Laura Herrtwich, Indrajit Nanda, Konstantinos Evangelou, et al.
Cell
|
August 25, 2018
DNA Damage Signaling Instructs Polyploid Macrophage Fate in Granulomas
Laura Herrtwich, Indrajit Nanda, Konstantinos Evangelou, et al.
Medrxiv : the Preprint Server for Health Sciences
|
April 10, 2026
<i>FRMPD4</i> , a causal gene for intellectual disability and epilepsy, is associated with X-linked non-syndromic hearing loss
Daniel Liedtke, Kristen Rak, Katrina M Schrode, et al.
American Journal of Human Genetics
|
April 30, 2013
ZC4H2 mutations are associated with arthrogryposis multiplex congenita and intellectual disability through impairment of central and peripheral synaptic plasticity
Hiromi Hirata, Indrajit Nanda, Anne van Riesen, et al.
Cytogenetic and Genome Research
|
August 19, 2015
Third Report on Chicken Genes and Chromosomes 2015
Michael Schmid, Jacqueline Smith, David W Burt, et al.
Page
of 6