C. Lai

No Association Between The Gly971 Arg Variant of the Insulin Receptor Substrate 1 Gene and NIDDM in the Taiwanese Population

Joanne I. Yeh, L. Chuang, C. Lai, 1996, Diabetes Care.

A novel forkhead-domain gene is mutated in a severe speech and language disorder

A. Monaco, F. Vargha-Khadem, S. Fisher, 2001 .

FOXP2 is not a major susceptibility gene for autism or specific language impairment.

G Baird, A. Bailey, G. Baird, 2002, American journal of human genetics.

The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorder.

A. Monaco, E. Green, F. Vargha-Khadem, 2000, American journal of human genetics.

Serotonin transporter (5-HTT) and gamma-aminobutyric acid receptor subunit beta3 (GABRB3) gene polymorphisms are not associated with autism in the IMGSA families. The International Molecular Genetic Study of Autism Consortium.

A. Bailey, E. Maestrini, E. Cook, 1999, American journal of medical genetics.

FOXP 2 Is Not a Major Susceptibility Gene for Autism or Specific Language Impairment

A. Bailey, G. Baird, P. Bolton, 2002 .