Mutations of cystic fibrosis transmembrane conductance regulator gene in patients with Mayer Rokitansky Kuster Hauser syndrome
Background and Objective: Mayer Rokitansky Kuster Hauser (MRKH) syndrome is characterized by Mullerian duct aplasia in an XX individual with female phenotype presenting primary amenorrhea at adolescence. This study was done to determine the mutations of cystic fibrosis transmembrane conductance regu...
| Main Authors: | , |
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| Format: | Article |
| Language: | fas |
| Published: |
Golestan University of Medical Sciences
2014-05-01
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| Series: | مجله دانشگاه علوم پزشکی گرگان |
| Subjects: | |
| Online Access: | http://goums.ac.ir/journal/browse.php?a_code=A-10-1-754&slc_lang=en&sid=1 |