Nature4d
22q11.2 microdeletion syndrome is a common cause of renal tract malformations
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 ...
Nature4d
Genotype–phenotype correlation in Smith-Magenis syndrome: Evidence that multiple genes in 17p11.2 contribute to the clinical spectrum
Purpose: Smith-Magenis syndrome (SMS) is a complex disorder ... On sequencing the RAI1 gene, SMS300 showed a heterozygous deletion of four bases, GCCG, starting from nucleotide 4933 that leads ...
CBS News5d
Judges in Jan. 6 cases and watchdog groups recoil at Justice Department's deletion of records
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 ...