Mitochondrial DNA mutations may not be frequent in patients with polycystic ovary syndrome

By Chen Ruixiang   Wang Huiling   Li Shaoping   Ren Yanfang  

Mitochondrial DNA, Vol. 24, Iss. 4, 2013-08 ,pp. : 418-419

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Altered Trace Mineral Milieu Might Play An Aetiological Role in the Pathogenesis of Polycystic Ovary Syndrome

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Biological Trace Element Research, Vol. 152, Iss. 1, 2013-04 ,pp. : 9-15

Humana Press, Inc

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A 9-bp Deletion Homoplasmy in Women with Polycystic Ovary Syndrome Revealed by Mitochondrial Genome-Mutation Screen

By Zhuo Guangchao   Feng Guofang   Leng Jianhang   Yu Lin   Jiang Yan  

Biochemical Genetics, Vol. 48, Iss. 1-2, 2010-02 ,pp. : 157-163

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Genetic variation in the vitamin D receptor gene and vitamin D serum levels in Egyptian women with polycystic ovary syndrome

By El-Shal Amal   Shalaby Sally   Aly Nader   Rashad Nearmeen   Abdelaziz Ahmed  

Molecular Biology Reports, Vol. 40, Iss. 11, 2013-11 ,pp. : 6063-6073

Springer Publishing Company

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Genetic variants in central metabolic genes influence some but not all relations of inflammatory markers in a collective with polycystic ovary syndrome

By Knebel Birgit   Lehr Stefan   Janssen Onno E.   Hahn Susanne   Nitzgen Ulrike   Jacob Sylvia   Haas Jutta   Muller-Wieland Dirk   Kotzka Jorg  

Archives of Physiology and Biochemistry, Vol. 118, Iss. 4, 2012-10 ,pp. : 219-229

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