Abstract: A method of ensuring that each newborn infant is identified at birth and maintaining the correct newborn and mother pairing at least until discharge of the mother and child. The method involves genotyping the infant and/or birth mother at one or more times.
Abstract: A method of ensuring that each newborn infant is identified at birth and maintaining the correct newborn and mother pairing at least until discharge of the mother and child. The method involves genotyping the infant and/or birth mother at one or more times.
Abstract: The present invention describes a process of DNA typing performed on human specimens utilizing a specific multiplex reaction which amplifies GATA short tandem repeats in the loci D18S535, D22S683, and D9S302 for the purpose of producing STR genotypes which may be used for identification purposes. This multiplex is an improvement over existing multiplex amplifications for STR typing in that it possesses an extremely high individualization potential for forensic studies and power of exclusion for parentage testing.