Mutations Causing Familial Biparental Hydatidiform Mole Implicate C6orf221 as a Possible Regulator of Genomic Imprinting in the Human Oocyte-Reference-Cited by-同舟云学术

Mutations Causing Familial Biparental Hydatidiform Mole Implicate C6orf221 as a Possible Regulator of Genomic Imprinting in the Human Oocyte

Published:2011-09 Issue:3 Volume:89 Page:451-458
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Parry David A.,Logan Clare V.,Hayward Bruce E.,Shires Michael,Landolsi Hanène,Diggle Christine,Carr Ian,Rittore Cécile,Touitou Isabelle,Philibert Laurent,Fisher Rosemary A.,Fallahian Masoumeh,Huntriss John D.,Picton Helen M.,Malik Saghira,Taylor Graham R.,Johnson Colin A.,Bonthron David T.,Sheridan Eamonn G.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

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