A Case of Molecular Analysis of XX Male Syndrome / 대한법의학회지
Korean Journal of Legal Medicine
;
: 38-41, 2013.
Article
Dans Coréen
| 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.
Texte intégral:
Disponible
Indice:
WPRIM (Pacifique occidental)
Sujet Principal:
Chromosome Y
/
Gène sry
/
Amélogénine
/
Caryotype
/
Syndrome de Klinefelter
Limites du sujet:
Femelle
/
Humains
/
Mâle
langue:
Coréen
Texte intégral:
Korean Journal of Legal Medicine
Année:
2013
Type:
Article
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