23
Sep
Silver-Russell Syndrome, 7p12 and the GRB10 gene
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Contribution of GRB10 to the prenatal phenotype in Silver-Russell syndrome? Lessons from 7p12 copy number variations. Silver-Russell syndrome (SRS) is a congenital disorder characterized by intrauterine growth restriction, poor growth after birth, relatively large head, a triangular face with a prominent forehead, body asymmetry and feeding difficulties. SRS is genetically... Read More
18
Sep
Learning more about genes associated with human diseases
Chromosome Disorder Outreach is asked frequently how to learn more about the genes associated with human diseases involved in any chromosome disorder. Here is a brief primer on how to search for more information. The Decipher Database is used mainly for information about which genes are located at a specific... Read More
