Estudo dos genes WNT4 E CTNNB1 na síndrome de MAYER-ROKITANSKY-KÜSTER-HAUSER

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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Bibliographic Details
Main Author:	Juliana Beaudette Drummond
Other Authors:	Luiz Armando Cunha De Marco
Format:	Others
Language:	Portuguese
Published:	Universidade Federal de Minas Gerais 2007
Online Access:	http://hdl.handle.net/1843/SMOC-733PBM

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