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Tim Morgan

Showing results (41-50 of 45) with videos related to

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European Journal of Human Genetics : EJHG|October 4, 2012
Vascular and connective tissue anomalies associated with X-linked periventricular heterotopia due to mutations in Filamin AEyal Reinstein, Sophia Frentz, Tim Morgan, et al.
American Journal of Medical Genetics. Part A|May 13, 2017
Autosomal dominant frontometaphyseal dysplasia: Delineation of the clinical phenotypeEmma M Wade, Zandra A Jenkins, Philip B Daniel, et al.
Nature Genetics|September 24, 2013
Mutations in genes encoding the cadherin receptor-ligand pair DCHS1 and FAT4 disrupt cerebral cortical developmentSilvia Cappello, Mary J Gray, Caroline Badouel, et al.
American Journal of Human Genetics|July 19, 2016
Mutations in MAP3K7 that Alter the Activity of the TAK1 Signaling Complex Cause Frontometaphyseal DysplasiaEmma M Wade, Philip B Daniel, Zandra A Jenkins, et al.
Nature Communications|July 7, 2017
A defect in myoblast fusion underlies Carey-Fineman-Ziter syndromeSilvio Alessandro Di Gioia, Samantha Connors, Norisada Matsunami, et al.
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Showing results (41-50 of 45) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 45 results.
European Journal of Human Genetics : EJHG|October 4, 2012
Vascular and connective tissue anomalies associated with X-linked periventricular heterotopia due to mutations in Filamin AEyal Reinstein, Sophia Frentz, Tim Morgan, et al.
American Journal of Medical Genetics. Part A|May 13, 2017
Autosomal dominant frontometaphyseal dysplasia: Delineation of the clinical phenotypeEmma M Wade, Zandra A Jenkins, Philip B Daniel, et al.
Nature Genetics|September 24, 2013
Mutations in genes encoding the cadherin receptor-ligand pair DCHS1 and FAT4 disrupt cerebral cortical developmentSilvia Cappello, Mary J Gray, Caroline Badouel, et al.
American Journal of Human Genetics|July 19, 2016
Mutations in MAP3K7 that Alter the Activity of the TAK1 Signaling Complex Cause Frontometaphyseal DysplasiaEmma M Wade, Philip B Daniel, Zandra A Jenkins, et al.
Nature Communications|July 7, 2017
A defect in myoblast fusion underlies Carey-Fineman-Ziter syndromeSilvio Alessandro Di Gioia, Samantha Connors, Norisada Matsunami, et al.
Pageof 5