Recurrent triploidy due to a failure to complete maternal meiosis II: whole-exome sequencing reveals candidate variants. [electronic resource]
Producer: 20151218Description: 339-46 p. digitalISSN:- 1460-2407
- 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
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
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