Charles Q. Tran

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

H. Zoghbi, U. Francke, R. Amir, 1999, Nature Genetics.

Influence of mutation type and X chromosome inactivation on Rett syndrome phenotypes

H. Zoghbi, O. Lichtarge, A. Philippi, 2000, Annals of neurology.

The human homologue (PEG3) of the mouse paternally expressed gene 3 (Peg3) is maternally imprinted but not mutated in women with familial recurrent hydatidiform molar pregnancies.

R. Slim, I. Veyver, Charles Q. Tran, 2001 .

The Human Homologue (PEG3) of the Mouse Paternally Expressed Gene 3 (Peg3) Is Maternally Imprinted But Not Mutated in Women With Familial Recurrent Hydatidiform Molar Pregnancies

R. Slim, I. B. Van den Veyver, Charles Q. Tran, 2001, The Journal of the Society for Gynecologic Investigation: JSGI.