Associated Papers
Variants in Maternal Effect Genes and Relaxed Imprinting Control in a Special Placental Mesenchymal Dysplasia Case with Mild Trophoblast Hyperplasia.
Huang TC et al.
Biomedicines, 2021
An analysis of mutational signatures of synonymous mutations across 15 cancer types.
Bin Y et al.
Bmc Medical Genetics, 2019
31815613 (PubMed )
Supplement: 12881_2019_926_MOESM2_ESM.xlsx › Neutral_synonymous_mutations
Novel Nonsense Mutation in the NLRP7 Gene Associated with Recurrent Hydatidiform Mole.
Ito Y et al.
Gynecologic and Obstetric Investigation, 2016
No evidence for mutations in NLRP7, NLRP2 or KHDC3L in women with unexplained recurrent pregnancy loss or infertility.
Aghajanova L et al.
Human Reproduction (oxford, England), 2015
No evidence for mutations in NLRP7 and KHDC3L in women with androgenetic hydatidiform moles.
Mahadevan S et al.
Prenatal Diagnosis, 2013
The p.L750V mutation in the NLRP7 gene is frequent in Mexican patients with recurrent molar pregnancies and is not associated with recurrent pregnancy loss.
Estrada H et al.
Prenatal Diagnosis, 2013
The genetics of recurrent hydatidiform moles in China: correlations between NLRP7 mutations, molar genotypes and reproductive outcomes.
Qian J et al.
Molecular Human Reproduction, 2011
Women heterozygous for NALP7/NLRP7 mutations are at risk for reproductive wastage: report of two novel mutations.
Qian J et al.
Human Mutation, 2007
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