Mutations causing familial biparental hydatidiform mole implicate c6orf221 as a possible regulator of genomic imprinting in the human oocyte.
Parry, David A
Mutations causing familial biparental hydatidiform mole implicate c6orf221 as a possible regulator of genomic imprinting in the human oocyte. [electronic resource] - American journal of human genetics Sep 2011 - 451-8 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
1537-6605
10.1016/j.ajhg.2011.08.002 doi
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
Mutations causing familial biparental hydatidiform mole implicate c6orf221 as a possible regulator of genomic imprinting in the human oocyte. [electronic resource] - American journal of human genetics Sep 2011 - 451-8 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
1537-6605
10.1016/j.ajhg.2011.08.002 doi
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