Associations of Polymorphisms in WNT9B and PBX1 with Mayer-Rokitansky-Küster-Hauser Syndrome in Chinese Han
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Title
Associations of Polymorphisms in WNT9B and PBX1 with Mayer-Rokitansky-Küster-Hauser Syndrome in Chinese Han
Authors
Keywords
Genetic loci, Sequence alignment, Wnt signaling cascade, Chinese people, Han Chinese people, Molecular genetics, Uterus, Etiology
Journal
PLoS One
Volume 10, Issue 6, Pages e0130202
Publisher
Public Library of Science (PLoS)
Online
2015-06-16
DOI
10.1371/journal.pone.0130202
References
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- SHOX duplications found in some cases with type I Mayer-Rokitansky-Kuster-Hauser syndrome
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- Designing Genome-Wide Association Studies: Sample Size, Power, Imputation, and the Choice of Genotyping Chip
- (2009) Chris C. A. Spencer et al. PLoS Genetics
- Identification and Functional Analysis of a New WNT4 Gene Mutation among 28 Adolescent Girls with Primary Amenorrhea and Müllerian Duct Abnormalities: A French Collaborative Study
- (2008) Pascal Philibert et al. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
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