Authors:
Amir, RE
Van den Veyver, IB
Schultz, R
Malicki, DM
Tran, CQ
Dahle, EJ
Philippi, A
Timar, L
Percy, AK
Motil, KJ
Lichtarge, O
Smith, EO
Glaze, DG
Zoghbi, HY
Citation: Re. Amir et al., Influence of mutation type and X chromosome inactivation on Rett syndrome phenotypes, ANN NEUROL, 47(5), 2000, pp. 670-679
Citation: Re. Amir et Hy. Zoghbi, Rett syndrome: Methyl-CpG-binding protein 2 mutations and phenotype-genotype correlations, AM J MED G, 97(2), 2000, pp. 147-152
Authors:
Buyse, IM
Fang, P
Hoon, KT
Amir, RE
Zoghbi, HY
Roa, BB
Citation: Im. Buyse et al., Diagnostic testing for Rett syndrome by DHPLC and direct sequencing analysis of the MECP2 gene: Identification of several novel mutations and polymorphisms, AM J HU GEN, 67(6), 2000, pp. 1428-1436
Authors:
Amir, RE
Van den Veyver, IB
Wan, M
Tran, CQ
Francke, U
Zoghbi, HY
Citation: Re. Amir et al., Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2, NAT GENET, 23(2), 1999, pp. 185-188
Authors:
Wan, MM
Lee, SSJ
Zhang, XY
Houwink-Manville, I
Song, HR
Amir, RE
Budden, S
Naidu, S
Pereira, JLP
Lo, IFM
Zoghbi, HY
Schanen, NC
Francke, U
Citation: Mm. Wan et al., Rett syndrome and beyond: Recurrent spontaneous and familial MECP2 mutations at CpG hotspots, AM J HU GEN, 65(6), 1999, pp. 1520-1529