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

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

Mosaics and moles

(2011) Lone Sunde et al.   EUROPEAN 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

Semen analysis by electron and fluorescence microscopy in a case of partial hydatidiform mole reveals a high incidence of abnormal morphology, diploidy, and tetraploidy

(2011) Katerina Chatzimeletiou et al.   FERTILITY AND STERILITY

Evolution and functional divergence of NLRP genes in mammalian reproductive systems

(2009) Xin Tian et al.   BMC EVOLUTIONARY BIOLOGY

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

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

Genetic and Epigenetic Analysis of Recurrent Hydatidiform Mole

(2009) Bruce E. Hayward et al.   HUMAN MUTATION

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

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

p57KIP2 immunostaining and molecular cytogenetics: combined approach aids in diagnosis of morphologically challenging cases with molar phenotype and in detecting androgenetic cell lines in mosaic/chimeric conceptions

(2007) Lori Hoffner et al.   HUMAN PATHOLOGY