Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 3 (of 3 Records) |
Query Trace: Mullerian Aplasia[original query] |
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Mutations in WNT4 are not responsible for Müllerian duct abnormalities in Chinese women. Reproductive biomedicine online 2012 Jun 24 (6): 630-3. Chang Xinyue, Qin Yingying, Xu Chengyan, Li Guangyu, Zhao Xiaoming, Chen Zi-Jia |
TBX6, LHX1 and copy number variations in the complex genetics of Müllerian aplasia. Orphanet journal of rare diseases 2013 8 (1): 125. Sandbacka Maria, Laivuori Hannele, Freitas Érika, Halttunen Mervi, Jokimaa Varpu, Morin-Papunen Laure, Rosenberg Carla, Aittomäki Kristii |
Copy number variation and regions of homozygosity analysis in patients with MÜLLERIAN aplasia. Molecular cytogenetics 2018 2 11 13. Demir Eksi Durkadin, Shen Yiping, Erman Munire, Chorich Lynn P, Sullivan Megan E, Bilekdemir Meric, Y?lmaz Elanur, Luleci Guven, Kim Hyung-Goo, Alper Ozgul M, Layman Lawrence |
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