S. Walsh

Lack of association between the apolipoprotein E epsilon4 allele (APOE epsilon4) and chronic schizophrenia.

R. Solomon, F. Crawford, T. Town, 1997, American journal of medical genetics.

Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossification

J. Hurst, S. Twigg, A. Wilkie, 2000, Nature Genetics.

Paternal origin of FGFR2 mutations in sporadic cases of Crouzon syndrome and Pfeiffer syndrome.

Rivka L. Glaser, E. Jabs, A. Wilkie, 2000, American journal of human genetics.

Paternal origin of FGFR2 mutations in sporadic cases of Crouzon and Pfeiffer syndromes.

E. Jabs, Diana S. Johnson, S. Boyadjiev, 1999 .

Dopamine DRD2/Cys311 is not associated with chronic schizophrenia.

R. Bradley, X. Cai, R. Solomon, 1996, American journal of medical genetics.

A comprehensive screen for TWIST mutations in patients with craniosynostosis identifies a new microdeletion syndrome of chromosome band 7p21.1.

L. Kearney, P. Njølstad, S. Twigg, 1998, American journal of human genetics.

Linkage of otopalatodigital syndrome type 2 (OPD2) to distal Xq28: evidence for allelism with OPD1.

S. Robertson, D. Becroft, M. Oldridge, 2001, American journal of human genetics.

Newly recognised craniosynostosis syndrome that does not map to known disease loci.

E. Blair, S. Wall, M. Oldridge, 2000, American journal of medical genetics.