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| 1 | Chromosome heteromorphisms: an impact on infertility显示文摘 | Feride Iffet Sahin Zerrin Yilmaz Ozge Ozalp Yuregir Tugce Bulakbasi Ozge Ozer Hulusi Bulent Zeyneloglu | 2008 | Journal of Assisted Reproduction and Genetics2008，，： | 1 |
| 2 | Antimicrobial activities of N-(2-hydroy- 1-naphthalidene)-amino acid (glycine, alanine, phenylalanine, histidine, tryptohuane) Schiff bases and their manganeses( III ) complexes显示文摘 | Iffet S Elef L Seza A | 2004 | Biometals2004，17，： | 1 |
| 3 | Chromosome heteromorphisms :an impact on infertility 显示文摘 | Feride Iffet Sahin Zerrin Yilmaz Ozge Ozalp Yuregir | 2008 | J Assist Reprod Genet2008，25，： | 1 |
| 4 | Chromosome heteromorphisms : an impact on infertility 显示文摘 | Feride Iffet Sahin Zerrin Yilmaz Ozge Ozalp Yuregir | 2008 | J Assist Reprod Genet2008，25，： | 1 |
| 5 | 45,XY,der(13;14)(q10;q10)in an azoospermic man with hypogonadotrophic hypogonadism显示文摘Dear Sir,I am Feride Iffet Sahin in Baskent University Facultyof Medicine,Department of Medical Genetics,Ankara,Turkey.We write to you about a case of 45,XY,der(13;14)(q10;q10) in an azoospermic man as a result of hypo-gonadotrophic hypogonadism.The most frequent form of Robertsonian transloca-tion is between chromosomes 13 and 14 [1].It is re-ported to be a cause of male infertility [2-4].The fre-quency of Robertsonian translocation among infertile menhas been reported to be 1%,which is higher than that ofthe normal newborn population [2,5].The translocatedchromosomes cause inappropriate pairing during malemeiosis and hinder normal sperm production,resultingin oligo-and azoospermia.A 34-year-old male patient was referred to the De-partment of Medical Genetics from the Department ofObstetrics and Gynecology,Baskent University Facultyof Medicine,for chromosome analysis and Y microdeletiontesting because of azoospermia as a result of hypogona-dotropic hypogonadism.During genetic counseling,we learned that the patientwas one of the seven children of a nonconsanguineousmarried couple.The patient's mother had no miscar-riages in her obstetric history.All his married siblings(three sisters and three brothers) had healthy children. | Ozge Ozalp Zerrin Yilmaz Esra Bulgan Kilicdag Filiz Bolat Tayfun Bagis Feride Iffet Sahin | 2006 | Asian Journal of Andrology2006，8，6： | 0 |
| 6 | 同一家庭3个姐妹色觉障碍(英文)显示文摘目的:评价我校医学生和她的家庭成员先天色觉障碍的遗传特征,以建立其遗传模式。方法:运用Ishihara(石原)假同色图试验测定色觉障碍,用FW100色调试验评估其类型。并进行眼科检查和遗传学研究,建立色盲家谱,并对她的家庭给予遗传学咨询。结果:眼科检测结果显示双眼最佳矫正视力为20/20(1.0),近视矫正屈光度-2D,裂隙灯检测和眼压测量结果在正常范围,眼底镜检查视神经、黄斑和周边视网膜均正常,其它外眼评估和神经学检测正常,先证者的姐妹和她父母的眼科检测也正常,3姐妹和父亲的IPPT试验错误得分为19~20/25,结果和红绿色盲中绿色觉异常者一致。染色体分析和卵巢周期均正常。结论:根据她家谱,她的色盲是伴X染色体的隐性外显率模式的遗传特征。 | Nimet ünay Gündogan Feride Iffet ■ahin ■ansal Gedik zge Pekdogan Yonca Akova | 2007 | 国际眼科杂志2007，7，4： | 0 |
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