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American Journal of Human Genetics
|
January 29, 2021
Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction
Joery den Hoed, Elke de Boer, Norine Voisin, et al.
Nature Communications
|
October 1, 2017
CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits
Aurélien Macé, Marcus A Tuke, Patrick Deelen, et al.
Human Brain Mapping
|
February 22, 2021
Effects of copy number variations on brain structure and risk for psychiatric illness: Large-scale studies from the ENIGMA working groups on CNVs
Ida E Sønderby, Christopher R K Ching, Sophia I Thomopoulos, et al.
Molecular Psychiatry
|
February 2, 2019
Correction: Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia
Ida E Sønderby, Ómar Gústafsson, Nhat Trung Doan, et al.
Molecular Psychiatry
|
October 5, 2018
Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia
Ida E Sønderby, Ómar Gústafsson, Nhat Trung Doan, et al.
Nature
|
September 2, 2011
Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus
Sébastien Jacquemont, Alexandre Reymond, Flore Zufferey, et al.
Nature
|
December 6, 2002
Initial sequencing and comparative analysis of the mouse genome
, Robert H Waterston, Kerstin Lindblad-Toh, et al.
Nature
|
June 16, 2007
Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project
, Ewan Birney, John A Stamatoyannopoulos, et al.
Science (New York, N.Y.)
|
April 25, 2009
The genome sequence of taurine cattle: a window to ruminant biology and evolution
, Christine G Elsik, Ross L Tellam, et al.
Page
of 17
Search research articles
Search
Showing results (161-170 of 169) with videos related to
Sort By:
Page
of 17
You have reached the last page of results.
This site can display upto 169 results.
American Journal of Human Genetics
|
January 29, 2021
Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction
Joery den Hoed, Elke de Boer, Norine Voisin, et al.
Nature Communications
|
October 1, 2017
CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits
Aurélien Macé, Marcus A Tuke, Patrick Deelen, et al.
Human Brain Mapping
|
February 22, 2021
Effects of copy number variations on brain structure and risk for psychiatric illness: Large-scale studies from the ENIGMA working groups on CNVs
Ida E Sønderby, Christopher R K Ching, Sophia I Thomopoulos, et al.
Molecular Psychiatry
|
February 2, 2019
Correction: Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia
Ida E Sønderby, Ómar Gústafsson, Nhat Trung Doan, et al.
Molecular Psychiatry
|
October 5, 2018
Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia
Ida E Sønderby, Ómar Gústafsson, Nhat Trung Doan, et al.
Nature
|
September 2, 2011
Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus
Sébastien Jacquemont, Alexandre Reymond, Flore Zufferey, et al.
Nature
|
December 6, 2002
Initial sequencing and comparative analysis of the mouse genome
, Robert H Waterston, Kerstin Lindblad-Toh, et al.
Nature
|
June 16, 2007
Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project
, Ewan Birney, John A Stamatoyannopoulos, et al.
Science (New York, N.Y.)
|
April 25, 2009
The genome sequence of taurine cattle: a window to ruminant biology and evolution
, Christine G Elsik, Ross L Tellam, et al.
Page
of 17