Authors:
Prasad, C
Prasad, AN
Chodirker, BN
Lee, C
Dawson, AK
Jocelyn, LJ
Chudley, AE
Citation: C. Prasad et al., Genetic evaluation of pervasive developmental disorders: the terminal 22q13 deletion syndrome may represent a recognizable phenotype, CLIN GENET, 57(2), 2000, pp. 103-109