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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

[226] 秦莹莹 , 赵涵 and 陈子江. Association of 8q22.3 locus in Chinese Han with idiopathic premature ovarian failure (POF）. Hum Mol Genet, 0, 2011.
[227] 秦莹莹. Younger poor ovarian response women achieved better pregnancy results in the first three IVF cycl.... Reproductive BioMedicine Online, 32, 532, 2016.
[228] 秦莹莹. Minichromosome maintenance complex component 8 mutations cause primary ovarian insufficienc. Fertility and Sterility, 106, 1485, 2016.
[229] 赵世斗 and 秦莹莹. The screening of HELQ gene in Chinese patients with premature ovarian failure. Reprod Biomed Online., 31, 573, 2015.
[230] 秦莹莹. Mutations in WNT4 are not responsible for Mullerian duct abnormalities in Chinese women. Reprod Biomed online, 24, 630, 2012.
[231] 秦莹莹. Association of basal serum testosterone levels with ovarian response and in vitro fertilization o.... Reproductive Biology and Endocrinology, 9, 9, 2011.
[232] 秦莹莹. Ethnic specificity of variants of the ESR1, HK3, BRSK1 genes and the 8q22.3 locus: No association.... Maturitas, 77, 64, 2013.
[233] 秦莹莹. Lack of association of WNT5A mutations with Müllerian duct abnormalities. . Reprod Biomed online, 26, 164, 2013.
[234] 马金龙 and 秦莹莹. The role of male chromosomal polymorphism played in spermatogenesis and the outcome of IVF/ICSI-E.... Int J Androl, 35, 802, 2012.
[235] 秦莹莹. Mutation analysis of NANOS3 in 80 Chinese and 88 Caucasian women with premature ovarian failure. fertil steril, 2007.
[236] 赵涵 and 秦莹莹. NOBOX homeobox mutation causes premature ovarian failure. Am J Hum Genet, 2007.
[237] 游力 and 秦莹莹. ESR1, HK3 and BRSK1 gene variants are associated with both age at natural menopause and premature.... Orphanet J Rare Dis, 7, 2012.
[238] 秦莹莹. Variants of the WNT7A gene in Chinese patients with müllerian duct abnormalities. fertil steril, 97, 391, 2011.
[239] 石玉华 , 赵跃然 , 陈子江 and 秦莹莹. Mutation Analysis of NOBOX homeodomain in Chinese Women with premature ovarian failure. Fertility and Sterility, 91, 1507, 2009.
[240] 陈子江 , 马金龙 and 秦莹莹. Analysis of PBX1 mutations in 192 Chinese women with Müllerian duct abnormalities. fertil steril, 95, 2615, 2011.

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