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秦莹莹 ( 主任医师 ) 赞
个人主页 http://faculty.sdu.edu.cn/qinyingying/zh_CN/index.htm
主任医师

论文成果当前位置：中文主页 >> 科学研究 >> 论文成果

[121] 秦莹莹 and 陈子江. Genetics of primary ovarian insufficiency: new developments and opportunitie. Hum Reprod Update, 2015.
[122] 秦莹莹. Younger poor ovarian response women achieved better pregnancy results in the first three IVF cycl.... Reproductive BioMedicine Online, 32, 532, 2016.
[123] 秦莹莹. Minichromosome maintenance complex component 8 mutations cause primary ovarian insufficienc. Fertility and Sterility, 106, 1485, 2016.
[124] 秦莹莹. Mutations in WNT4 are not responsible for Mullerian duct abnormalities in Chinese women. Reprod Biomed online, 24, 630, 2012.
[125] 秦莹莹. Association of basal serum testosterone levels with ovarian response and in vitro fertilization o.... Reproductive Biology and Endocrinology, 9, 9, 2011.
[126] 陈子江 and 秦莹莹. FMR1 Premutation Is an Uncommon Explanation for Premature Ovarian Failure in Han Chinese. Plos one, 2014.
[127] 陈子江 , 秦莹莹 and 游力. Mutations in HOXA11 are not responsible for Müllerian duct anomalies in Chinese patients. Reprod Biomed online, 2014.
[128] 秦莹莹 and 陈子江. Novel WT1 Missense Mutations in Han Chinese Women with Premature Ovarian Failure. SCI REP, 2015.
[129] 崔琳琳 , 秦莹莹 and 陈子江. Novel mutations in the TP63 gene are potentially associated with Müllerian duct anomalies. Human reproduction, 2016.
[130] 陈子江 , 秦莹莹 and 崔琳琳. Chronic Pelvic Inflammation Diminished Ovarian Reserve as Indicated by Serum Anti Mülerrian Hormo.... Plos one, 2016.
[131] 陈子江 , 秦莹莹 and 张浩波. Mutations in KISS1 are not responsible for idiopathic hypogonadotropic hypogonadism in Chinese pa.... J Assist Reprod Genet, 2015.
[132] 陈子江 and 秦莹莹. Risks associated with premature ovarian failure in Han Chinese women. Reprod Biomed online, 2015.
[133] 陈子江 , 赵世斗 and 秦莹莹. MicroRNA-22-3p is down-regulated in the plasma of Han Chinese patients with premature ovarian fai.... fertil steril, 2015.
[134] 陈子江 and 秦莹莹. Transcription factor SOHLH1 potentially associated with primary ovarian insufficiency. fertil steril, 2015.
[135] 秦莹莹 and 陈子江. Novel variants in the SOHLH2 gene are implicated in human premature ovarian failure. fertil steril, 2014.

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