位置：成果数据库 > 期刊 > 期刊详情页
LHX1 Mutation Screening in 96 Patients with Müllerian Duct Abnormalities
  • ISSN号：0015-0282
  • 期刊名称：Fertility and Sterility
  • 时间：0
  • 页码：682-685
  • 相关项目：PTEN-PI3K-Akt信号通路及其下游基因FOXO3A在卵巢早衰发病中的作用
作者： Mingdi Xia|Han Zhao|Yingying Qin|Yulan Mu|Jia Wang|Jinglong Ma|Zi-Jiang Chen|
同期刊论文项目
PTEN-PI3K-Akt信号通路及其下游基因FOXO3A在卵巢早衰发病中的作用
期刊论文 27
同项目期刊论文
Morphologically abnormal oocytes not capable of fertilization despite repeated strategies
Dynamic modulation of cytoskeleton during in vitro maturation in human oocytes
PTEN gene analysis in premature ovarian failure patients
Evaluation of the developmental potential of metaphase I oocytes from stimulated intracytoplasmic sp
Association of basal serum testosterone levels with ovarian response and in vitro fertilization outc
Positive and Negative Feedback Regulation in the Production and Secretion of Insulin from INS-1 Cell
Genome-wide association study identifies susceptibility loci for polycystic ovary syndrome on chromo
Genotype–phenotype correlations of PCOS susceptibility SNPs identified by GWAS in a large coho
Variants of the WNT7A gene in Chinese patients with m€ullerian duct abnormalities
苗勒管发育异常对生育结局的影响及HOXA13基因的突变研究
Identification of YAP1 as a Novel Susceptibility Gene for Polycystic Ovary Syndrome
Lack of association of WNT5A mutations with Müllerian duct abnormalities
PAX2 in 192 Chinese women with Müllerian duct abnormalities: mutation analysis
Association Study of Gene LPP in Women with Polycystic Ovary Syndrome. .2012; 7(10):e46370
ESR1, HK3 and BRSK1 gene variants are associated with both age at natural menopause and premature ov
Mutations in WNT4 are not responsible for Müllerian duct abnormalities in Chinese women
A Genome-wide Association Study Reveals that Variants within the HLA Region Are Associated with Risk
The role of male chromosomal polymorphism played in spermatogenesis and the outcome of IVF⁄ICS
Family-based analysis of susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p2