Had the temperature been a few degrees higher, had the sun passed farther across the sky, Tuesday August 18, 2015, could have ...
Noonan syndrome with multiple lentigines (NSML) is a rare autosomal dominant disorder, primarily caused by variants in the PTPN11 gene. Characterized by multiple lentigines, hypertelorism, short ...
These tumors are not cancer. Noonan syndrome. This condition affects many parts of the body. Children with Noonan syndrome may be short and have wide-set eyes, heart defects, and bleeding problems.
New research revealing the fingerprints of Sudden Infant Death Syndrome within blood samples could open the door to simple tests to identify babies at risk. New University of Virginia School of ...
What are records? Since 2014, The Marshall Project has been curating some of the best criminal justice reporting from around the web. In these records you will find the most recent and the most ...
New University of Virginia School of Medicine research revealing the fingerprints of Sudden Infant Death Syndrome (SIDS ... door to simple tests to identify babies at risk. The research is ...
It could have meant a lifetime of grief, of heartache. Instead, it meant flashbacks, searing guilt. But also a saved life — her child’s. The Aussie mum had inadvertently left her baby daughter locked ...
Metabolic syndrome is a constellation of conditions that together increase the risk of type 2 diabetes, stroke, and cardiovascular problems, including heart attack. The features of metabolic syndrome ...
Gianni Rodari used puns, topsy-turvyism and zany names to invent stories for children and help children invent their own. By Mac Barnett For the three Latino kids transported to 1862 Mexico in ...
John Noonan is a former staffer on defense and armed-service committees in the House and Senate, a veteran of the United States Air Force, and a senior adviser to POLARIS National Security.
Although Noonan syndrome was thought unlikely, the PTPN11 gene was analysed with no mutation found. The HRAS gene was analysed in view of the phenotypic overlap between CFC and CS. Mutation analysis ...
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