The molecular basis of the renal malformation is unknown; deletion of one or more genes could be responsible. The 22q11.2 microdeletion syndrome is a frequent cause of kidney malformation and ...

[Analysis of a twin pregnancy with false negative result for 22q11.2 deletion syndrome by expanded non-invasive prenatal testing]. [Discussion on the status quo and solutions to the prevention and ...

Purpose: Smith-Magenis syndrome ... she has 2-3 toe syndactyly, mild clinodactyly of fifth fingers, and lax joints. On sequencing the RAI1 gene, SMS300 showed a heterozygous deletion of four ...

Some eight years since the Nintendo Switch was released, we have finally got an official look at the Nintendo Switch 2. In a rather brief trailer, Nintendo showed off its next-generation gaming ...

In an opinion issued Thursday, U.S. District court judge Paul Friedman noted the deletion of the public information by the acting Justice Department leadership. Friedman included a recent version ...