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Structural genomic variation as risk factor for idiopathic recurrent miscarriage.
Nagirnaja L, Palta P, Kasak L, Rull K, Christiansen OB, Nielsen HS, Steffensen R, Esko T, Remm M, Laan M. Nagirnaja L, et al. Hum Mutat. 2014 Aug;35(8):972-82. doi: 10.1002/humu.22589. Epub 2014 Jun 24. Hum Mutat. 2014. PMID: 24827138 Free PMC article.
Recurrent miscarriage (RM) is a multifactorial disorder with acknowledged genetic heritability that affects 3% of couples aiming at childbirth. ...The CNV disrupts PDZD2 and GOLPH3 genes predominantly expressed in placenta and it may represent a novel risk …
Recurrent miscarriage (RM) is a multifactorial disorder with acknowledged genetic heritability that affects 3% of couples aimi …
Analysis of C3 Gene Variants in Patients With Idiopathic Recurrent Spontaneous Pregnancy Loss.
Mohlin FC, Gros P, Mercier E, Gris JR, Blom AM. Mohlin FC, et al. Front Immunol. 2018 Aug 7;9:1813. doi: 10.3389/fimmu.2018.01813. eCollection 2018. Front Immunol. 2018. PMID: 30131807 Free PMC article.
Miscarriage is the most common complication of pregnancy. Approximately 1% of couples trying to conceive will experience recurrent miscarriages, defined as three or more consecutive pregnancy losses and many of these cases remain idiopathic. ...We performed f …
Miscarriage is the most common complication of pregnancy. Approximately 1% of couples trying to conceive will experience recurrent …