Recurrent triploidy due to a failure to complete maternal meiosis II: whole-exome sequencing reveals candidate variants.

Filges, I

Recurrent triploidy due to a failure to complete maternal meiosis II: whole-exome sequencing reveals candidate variants. [electronic resource] - Molecular human reproduction Apr 2015 - 339-46 p. digital

Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

1460-2407

10.1093/molehr/gau112 doi


Abnormal Karyotype
Abortion, Habitual--diagnosis
Adult
Exome
Female
Gene Expression
Genetic Predisposition to Disease
Genotype
High-Throughput Nucleotide Sequencing
Humans
Meiosis
Mutation
Pedigree
Phenotype
Phospholipase C delta--genetics
Pregnancy
Receptors, Steroid--genetics
Sequence Analysis, DNA
Triploidy
Oxysterol Binding Proteins