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MTHFR C677T and A1298C Genotypes and Haplotypes in Slovenian Couples with Unexplained Infertility Problems and in Embryonic Tissues from Spontaneous Abortions

机译：mTHFR C677T和a1298C基因型和单倍型在斯洛文尼亚夫妇中有不明原因的不孕问题和胚胎组织中的自然流产

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Š Stangler Herodež; B Zagradišnik; A Erjavec Škerget; A Zagorac; I Takač; V Vlaisavljević; L Lokar; N Kokalj Vokač;
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1. MTHFR C677T AND A1298C GENOTYPES AND HAPLOTYPES IN SLOVENIAN COUPLES WITH UNEXPLAINED INFERTILITY PROBLEMS AND IN EMBRYONIC TISSUES FROM SPONTANEOUS ABORTIONS [J] . Stangler Herodez S, Zagradisnik B, Erjavec Skerget A, Balkan journal of medical genetics: BJMG . 2013,第1期

机译：斯洛文尼亚夫妇的MTHFR C677T和A1298C基因型和单倍型存在无法解释的不育性问题和自然流产的胚胎组织
2. MTHFR C677T and A1298C Genotypes and Haplotypes in Slovenian Couples with Unexplained Infertility Problems and in Embryonic Tissues from Spontaneous Abortions [J] . A Erjavec ?kerget, A Zagorac, B Zagradi?nik, Balkan journal of medical genetics: BJMG . 2013,第1期

机译：MTHFR C677T和A1298C基因型和单倍型的斯洛文尼亚夫妇与无法解释的不育问题和自然流产的胚胎组织中。
3. Genotypes of the C677T and A1298C polymorphisms of the MTHFR gene as a cause of human spontaneous embryo loss. [J] . Callejon G, Mayor-Olea A, Jimenez AJ, Human Reproduction . 2007,第12期

机译：MTHFR基因的C677T和A1298C多态性的基因型是人类自发性胚胎丢失的原因。
4. Two different approaches for the study of nk cells receptors in unexplained recurrent spontaneous abortions (ursa) [C] . Konsta E., Kitsiou V., Psarra K., European Congress of Immunology . 2009

机译：两种不同的方法，用于研究未解释的经常性自发性流产（URSA）中的NK细胞受体
5. MTHFRC677T and A1298C Genotypes and Haplotypes in Slovenian Couples with Unexplained Infertility Problems and in Embryonic Tissues from Spontaneous Abortions [O] . Š Stangler Herodež, B Zagradišnik, A Erjavec Škerget, 2013

机译：甲基四氢呋喃斯洛文尼亚夫妇患有无法解释的不育问题以及自然流产的胚胎组织中的C677T和A1298C基因型和单倍型
6. Prevalence of the polymorphism MTHFR A1298C and not MTHFR C677T is related to chromosomal aneuploidy in Brazilian Turner Syndrome patients A prevalência do polimorfismo A1298C e não do C677T do gene MTHFR está relacionada à ocorrência de aneuploidias cromossômicas em mulheres brasileiras portadoras da síndrome de Turner [O] . Kelly Cristina de Oliveira, Bianca Bianco, Ieda T. N. Verreschi, 2008

机译：巴西特纳氏综合症患者多态性MTHFR A1298C而不是MTHFR C677T的发生与染色体非整倍性有关MTHFR基因多态性A1298C而非C677T的发生与巴西患有Turn综合征的妇女的染色体非整倍性有关

MTHFR C677T and A1298C Genotypes and Haplotypes in Slovenian Couples with Unexplained Infertility Problems and in Embryonic Tissues from Spontaneous Abortions

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