Sinnett D.,1988
Sinnett D., Lavergne L., Melancon S.B., Dallaire L., Potier M., Labuda D. Lesch-Nyhan syndrome: molecular investigation of three French Canadian families using a hypoxanthine-guanine phosphoribosyltransferase cDNA probe. - Hum.Genet., 1988, v. 81, p. 4-8.
