1.
Korean Journal of Legal Medicine
;
: 38-41, 2013.
Article
in Korean
| WPRIM
| ID: wpr-34173
ABSTRACT
Sex typing may become the start point in investigations that are usually performed through amelogenin typing. In cases involving genotype-phenotype discrepancy, amelogenin typing could yield misleading results. The rare XX male syndrome is characterized by a phenotypic male with a 46, XX female karyotype. In this point, this case report would help understand the importance of genotype-phenotype discrepancy.