AJHG

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AJHGAmerican Journal of Human Genetics
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References in periodicals archive ?
Riazuddin et al., "Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23," The American Journal of Human Genetics, vol.
Goldstein et al., "Dating the origin of the CCR5-A32 AIDS-resistance allele by the coalescence of haplotypes," American Journal of Human Genetics, vol.
Mundlos et al., "Acromesomelic dysplasia maroteaux type maps to human chromosome 9," American Journal of Human Genetics, vol.
Hodges et al., "Disrtruption of a novel imprinted zinc-finger gene, ZNF215, in Beckwith-Wiedemann syndrome," American Journal of Human Genetics, vol.
The results of the study, published in the American Journal of Human Genetics, showed 15 genes in which mutations cluster closely together, 12 of which were associated with developmental disorders.
The American Journal of Human Genetics recently published a study sequencing genomes from ancient Canaanites and modern day Lebanese, finding a direct link.
Lu et al., "A specific IFIH1 gain-of-function mutation causes singleton-merten syndrome," The American Journal of Human Genetics, vol.
Tran-Fadulu et al., "Mutations in smooth muscle alpha-actin (ACTA2) cause coronary artery disease, stroke, and Moyamoya disease, along with thoracic aortic disease," The American Journal of Human Genetics, vol.
[allowing the] team to pinpoint the common genetic origin of different populations and to get a better grasp on the history of migration in Tibet." Among others engaged in related research has been Shuhua Xu, a population geneticist at the Chinese Institute of Sciences' Shanghai Institutes for Biological Sciences, who published research in September in the American Journal of Human Genetics.
The study involved 3,200 subjects and was published online May 23,2016 in the American Journal of Human Genetics.
Publishing in the American Journal of Human Genetics, first author and PhD student Charlotte Alston described the technique, which has already identified six patients from four families affected by this form of mitochondrial disease.
Publishing in the American Journal of Human Genetics, PhD student Charlotte Alston described the technique, which has already identified six patients from four families affected by this form of disease.
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