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American Journal of Human Genetics
|
August 16, 2016
GNB5 Mutations Cause an Autosomal-Recessive Multisystem Syndrome with Sinus Bradycardia and Cognitive Disability
Elisabeth M Lodder, Pasquelena De Nittis, Charlotte D Koopman, et al.
Human Mutation
|
December 2, 2017
Inactivation of AMMECR1 is associated with growth, bone, and heart alterations
Mariana Moysés-Oliveira, Giuliana Giannuzzi, Richard J Fish, et al.
American Journal of Human Genetics
|
January 2, 2018
KIAA1109 Variants Are Associated with a Severe Disorder of Brain Development and Arthrogryposis
Lucie Gueneau, Richard J Fish, Hanan E Shamseldin, et al.
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of 42
Search research articles
Search
Showing results (411-420 of 413) with videos related to
Sort By:
Page
of 42
You have reached the last page of results.
This site can display upto 413 results.
American Journal of Human Genetics
|
August 16, 2016
GNB5 Mutations Cause an Autosomal-Recessive Multisystem Syndrome with Sinus Bradycardia and Cognitive Disability
Elisabeth M Lodder, Pasquelena De Nittis, Charlotte D Koopman, et al.
Human Mutation
|
December 2, 2017
Inactivation of AMMECR1 is associated with growth, bone, and heart alterations
Mariana Moysés-Oliveira, Giuliana Giannuzzi, Richard J Fish, et al.
American Journal of Human Genetics
|
January 2, 2018
KIAA1109 Variants Are Associated with a Severe Disorder of Brain Development and Arthrogryposis
Lucie Gueneau, Richard J Fish, Hanan E Shamseldin, et al.
Page
of 42