No evidence for mutations inNLRP7andKHDC3Lin women with androgenetic hydatidiform moles

Report of four new patients with protein-truncating mutations in C6orf221/KHDC3L and colocalization with NLRP7

(2012) Ramesh Reddy et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Mutations inNLRP7are associated with diploid biparental hydatidiform moles, but not androgenetic complete moles

(2012) Peter H Dixon et al.   JOURNAL OF MEDICAL GENETICS

Mosaic moles and non-familial biparental moles are not caused by mutations in NLRP7, NLRP2 or C6orf221

(2012) L. Andreasen et al.   MOLECULAR HUMAN REPRODUCTION

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

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

What a difference an egg makes

(2011) Rosemary A Fisher et al.   LANCET

The genetics of recurrent hydatidiform moles in China: correlations between NLRP7 mutations, molar genotypes and reproductive outcomes

(2011) JianHua Qian et al.   MOLECULAR HUMAN REPRODUCTION

NLRP7 and the genetics of post-molar choriocarcinomas in Senegal

(2011) Rima Slim et al.   MOLECULAR HUMAN REPRODUCTION

Recurrent triploid and dispermic conceptions in patients with NLRP7 mutations

(2011) R. Slim et al.   PLACENTA

Evolution and functional divergence of NLRP genes in mammalian reproductive systems

(2009) Xin Tian et al.   BMC EVOLUTIONARY BIOLOGY

Germline Mutation in NLRP2 (NALP2) in a Familial Imprinting Disorder (Beckwith-Wiedemann Syndrome)

(2009) Esther Meyer et al.   PLoS Genetics

Expression Analysis of the NLRP Gene Family Suggests a Role in Human Preimplantation Development

(2008) Pu Zhang et al.   PLoS One