American Journal of Medical Genetics is a peer-reviewed medical journal dealing with human genetics published in three separate sections (parts) by Wiley-Liss: Until 1996 they were one journal under the name American Journal of Medical Genetics, when they split into Part A and Part B. Part C was established in 1999.
The first U.S. population prevalence study of mutations in the gene that causes fragile X syndrome, the most common inherited form of intellectual disability, suggests the mutation in the gene – and its associated health ...
Jun 14, 2012
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Published in the American Journal of Medical Genetics, a University of Minnesota Medical School study found that it is normal for children with Fanconi anemia to be shorter and thinner than other children. Fanconi anemia ...
Feb 26, 2024
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Today's substance use prevention efforts ignore individual genetic risk, but new Rutgers University research suggests that DNA test results may eventually enhance prevention and treatment and improve outcomes.
May 30, 2023
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There is a link between ADHD and dietary habits. This is shown in a new study by Örebro researchers, published in the American Journal of Medical Genetics.
Oct 21, 2020
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A study funded by the Veterans Administration and directed by researchers at the University of Miami Miller School of Medicine has shown few differences in the profiles of genes that influence cognition between people with ...
Jan 22, 2020
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When expectant parents learn their child will be born with Down syndrome, they invariably have questions about what this diagnosis will mean for their son or daughter and for the rest of their family. When will their child ...
Jan 2, 2019
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Fetal magnetic resonance imaging (MRI) can reliably spot holoprosencephaly as early as 18 gestational weeks, providing an opportunity to counsel families earlier in their pregnancy, according to Children's-led research published ...
May 21, 2018
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Researchers at the Human Genome Sequencing Center at Baylor College of Medicine have conducted a study of 20 individuals with Xia-Gibbs syndrome, a rare condition that has symptoms of severe developmental delay, sleep apnea, ...
May 7, 2018
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PHP1A (pseudohypoparathyroidism 1A) is a rare genetic disorder that causes short adult stature, multi-hormone resistance, early-onset obesity and cognitive impairment.
Feb 14, 2018
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Mike and Julie were eagerly counting down the days until they'd get to meet their baby girl, Emma. But hours after her birth, their joy turned to worry. Doctors had made a discovery that shocked them: Their newborn daughter ...
Oct 23, 2017
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