Fiona Francis

Autism and multiple exostoses associated with an X;8 translocation occurring within the GRPR gene and 3' to the SDC2 gene.

P. Bolton, A. Monaco, H. Willard, 1997, Human molecular genetics.

A 6-Mb YAC contig in Xp22.1-p22.2 spanning the DXS69E, XE59, GLRA2, PIGA, GRPR, CALB3, and PHKA2 genes.

D. Schlessinger, H. Willard, J. Kere, 1995, Genomics.

Isolation of a putative transcriptional regulator from the region of 22q11 deleted in DiGeorge syndrome, Shprintzen syndrome and familial congenital heart disease.

I. Dunham, C. Roberts, A. Baldini, 1993, Human molecular genetics.

Characterization of the C3 YAC contig from proximal mouse chromosome 17 and analysis of allelic expression of genes flanking the imprinted Igf2r gene.

S. Meier-Ewert, H. Lehrach, R. Cox, 1997, Genomics.

Genomic organization of a 225-kb region in Xq28 containing the gene for X-linked myotubular myopathy (MTM1) and a related gene (MTMR1).

A. Poustka, S. Wiemann, A. Rosenthal, 1998, Genomics.

Distribution of mutations in the PEX gene in families with X-linked hypophosphataemic rickets (HYP).

T. Meitinger, T. Strom, H. Lehrach, 1997, Human molecular genetics.