A Case of Molecular Analysis of XX Male Syndrome / 대한법의학회지
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.
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Y Chromosome
/
Genes, sry
/
Amelogenin
/
Karyotype
/
Klinefelter Syndrome
Limits:
Female
/
Humans
/
Male
Language:
Korean
Journal:
Korean Journal of Legal Medicine
Year:
2013
Type:
Article
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