The p.L750V mutation in theNLRP7gene is frequent in Mexican patients with recurrent molar pregnancies and is not associated with recurrent pregnancy loss

Mutations Causing Familial Biparental Hydatidiform Mole Implicate C6orf221 as a Possible Regulator of Genomic Imprinting in the Human Oocyte

(2011) David A. Parry et al.   AMERICAN JOURNAL OF HUMAN GENETICS

The spectrum of NLRP7 mutations in French patients with recurrent hydatidiform mole

(2011) Joël Muhlstein et al.   European Journal of Obstetrics & Gynecology and Reproductive Biology

NLRP7 in the spectrum of reproductive wastage: rare non-synonymous variants confer genetic susceptibility to recurrent reproductive wastage

(2011) C. Messaed et al.   JOURNAL OF MEDICAL GENETICS

Heterogeneity in recurrent complete hydatidiform mole: Presentation of two new Turkish families with different genetic characteristics

(2010) S. Buyukkurt et al.   PLACENTA

NLRP7 mutations in women with diploid androgenetic and triploid moles: a proposed mechanism for mole formation

(2009) C. Deveault et al.   HUMAN MOLECULAR GENETICS

Identification of 13 novel NLRP7 mutations in 20 families with recurrent hydatidiform mole; missense mutations cluster in the leucine-rich region

(2009) C M Wang et al.   JOURNAL OF MEDICAL GENETICS