A Case of Molecular Analysis of XX Male Syndrome / 대한법의학회지
Korean Journal of Legal Medicine
;
: 38-41, 2013.
Artigo
em Coreano
| 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.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Cromossomo Y
/
Genes sry
/
Amelogenina
/
Cariótipo
/
Síndrome de Klinefelter
Limite:
Feminino
/
Humanos
/
Masculino
Idioma:
Coreano
Revista:
Korean Journal of Legal Medicine
Ano de publicação:
2013
Tipo de documento:
Artigo
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