American Journal of Medical Genetics Part A
Article . 2015 . Peer-reviewed
License: Wiley Online Library User Agreement
Data sources: Crossref
Novel de novo mutations in EFTUD2 detected by exome sequencing in mandibulofacial dysostosis with Microcephaly syndrome
Authors: Arindam, Sarkar; Lisa T, Emrick; Eboni M, Smith; Elise G, Austin; Yaping, Yang; Jill V, Hunter; Fernando, Scaglia; +1 Authors
Arindam, Sarkar; Lisa T, Emrick; Eboni M, Smith; Elise G, Austin; Yaping, Yang; Jill V, Hunter; Fernando, Scaglia; Seema R, Lalani;
doi: 10.1002/ajmg.a.36948
pmid: 25735261
Novel de novo mutations in EFTUD2 detected by exome sequencing in mandibulofacial dysostosis with Microcephaly syndrome
Related Organizations
- Boston Children's Hospital United States
- Baylor College of Medicine United States
Keywords
Male, Heterozygote, DNA Mutational Analysis, Syndrome, Peptide Elongation Factors, Radiography, Codon, Nonsense, Child, Preschool, Microcephaly, Humans, Abnormalities, Multiple, Exome, Female, Genetic Association Studies, Mandibulofacial Dysostosis, Ribonucleoprotein, U5 Small Nuclear
Male, Heterozygote, DNA Mutational Analysis, Syndrome, Peptide Elongation Factors, Radiography, Codon, Nonsense, Child, Preschool, Microcephaly, Humans, Abnormalities, Multiple, Exome, Female, Genetic Association Studies, Mandibulofacial Dysostosis, Ribonucleoprotein, U5 Small Nuclear
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citations
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This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
popularity
Popularity provided by BIP!
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
16
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