Mutations causing familial biparental hydatidiform mole implicate c6orf221 as a possible regulator of genomic imprinting in the human oocyte. [electronic resource]
Producer: 20111122Description: 451-8 p. digitalISSN:- 1537-6605
- Adaptor Proteins, Signal Transducing -- genetics
- Base Sequence
- Cell Line
- Female
- Genes, Recessive -- genetics
- Genomic Imprinting -- genetics
- Humans
- Hydatidiform Mole -- genetics
- Immunohistochemistry
- Molecular Sequence Data
- Mutation -- genetics
- Oocytes -- metabolism
- Pedigree
- Pregnancy
- Proteins -- genetics
- Sequence Alignment
- Sequence Analysis, DNA
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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