F1000Research

Journal of minimally invasive gynecology

human reproduction (oxford, england)

journal of cellular physiology

the kaohsiung journal of medical sciences

[1] Analysis of in fetal growth restriction and pregnancy loss.

[2] The lncRNA CCAT2 rs6983267 G allele is associated with decreased susceptibility to recurrent miscarriage.

[3] Increased Fetal Chromosome Detection with the Use of Operative Hysteroscopy During Evacuation of Products of Conception for Diagnosed Miscarriage.

[4] Disordered p53-MALAT1 pathway is associated with recurrent miscarriage.

[5] Pigment epithelium-derived factor, a novel decidual natural killer cells-derived factor, protects decidual stromal cells via anti-inflammation and anti-apoptosis in early pregnancy.

[6] role of 1,25-dihydroxyvitamin d (vitamin d3) as immunomodulator in recurrent missed miscarriage

[7] maternal methyltetrahydrofolate reductase gene mutation in patients with missed abortions

[8] Determining the Cause of Recurrent Miscarriages in a Couple: Importance of NOR in the Era of NGS.

[9] Differential global and MTHFR gene specific methylation patterns in preeclampsia and recurrent miscarriages: A case-control study from North India.

[10] The lncRNA CCAT2 rs6983267 G allele is associated with decreased susceptibility to recurrent miscarriage.

[11] Performance of preimplantation genetic testing for aneuploidy in IVF cycles for patients with advanced maternal age, repeat implantation failure, and idiopathic recurrent miscarriage.

[12] Disordered p53-MALAT1 pathway is associated with recurrent miscarriage.

[13] Genetics of recurrent miscarriage and fetal loss

[14] Genetics of recurrent miscarriage: Challenges, current knowledge, future directions

[15] The Attenuation of Trophoblast Invasion Caused by the Downregulation of EZH2 Is Involved in the Pathogenesis of Human Recurrent Miscarriage

[16] Hyaluronan–binding protein 2 (HABP2) gene variation in women with recurrent miscarriage

[17] Multiple occurrence of psychomotor retardation and recurrent miscarriages in a family with a submicroscopic reciprocal translocation t(7;17)(p22;p13.2)

[18] CHROMOSOMAL ABNORMALITIES IN PATIENTS WITH RECURRENT MISCARRIAGE

[19] Copy number variations in miscarriage products and their relationship with consanguinity and recurrent miscarriage in individuals with normal karyotypes.