Estudo dos genes WNT4 E CTNNB1 na síndrome de MAYER-ROKITANSKY-KÜSTER-HAUSER
=== The Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is a congenital malformation of the female genital tract and is the second cause of primary amenorrhea, affecting one in every 5000 female live births. The genetic defect associated with the Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome has no...
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| Format: | Others |
| Language: | Portuguese |
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Universidade Federal de Minas Gerais
2007
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| Online Access: | http://hdl.handle.net/1843/SMOC-733PBM |