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Showing results (71-80 of 75) with videos related to

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Cell|September 27, 2016
Mutations in Human Accelerated Regions Disrupt Cognition and Social BehaviorRyan N Doan, Byoung-Il Bae, Beatriz Cubelos, et al.
Nature Genetics|October 5, 2001
The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosisY Yang, A Hentati, H X Deng, et al.
American Journal of Human Genetics|May 3, 2011
Human mutations in NDE1 cause extreme microcephaly with lissencephaly [corrected]Fowzan S Alkuraya, Xuyu Cai, Carina Emery, et al.
Annals of Neurology|January 4, 2012
A novel X-linked disorder with developmental delay and autistic featuresNamik Kaya, Dilek Colak, Albandary Albakheet, et al.
Neuron|January 29, 2013
Using whole-exome sequencing to identify inherited causes of autismTimothy W Yu, Maria H Chahrour, Michael E Coulter, et al.
Pageof 8

Showing results (71-80 of 75) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 75 results.
Cell|September 27, 2016
Mutations in Human Accelerated Regions Disrupt Cognition and Social BehaviorRyan N Doan, Byoung-Il Bae, Beatriz Cubelos, et al.
Nature Genetics|October 5, 2001
The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosisY Yang, A Hentati, H X Deng, et al.
American Journal of Human Genetics|May 3, 2011
Human mutations in NDE1 cause extreme microcephaly with lissencephaly [corrected]Fowzan S Alkuraya, Xuyu Cai, Carina Emery, et al.
Annals of Neurology|January 4, 2012
A novel X-linked disorder with developmental delay and autistic featuresNamik Kaya, Dilek Colak, Albandary Albakheet, et al.
Neuron|January 29, 2013
Using whole-exome sequencing to identify inherited causes of autismTimothy W Yu, Maria H Chahrour, Michael E Coulter, et al.
Pageof 8