Lahat E., Heyman E., Barkay A., et al: Asymmetric crying facies and associated congenital anomalies: Prospective study and review of the literature. J Child Neurol2000;15:808-810.
2.
Silengo MC, Bell GL, Biagioli M., et al: Asymmetric crying facies with microcephaly and mental retardation. An autosomal dominant syndrome with variable expressivity. Clin Genet1986;30:481-484.
3.
Thomas JA, Graham JM: Chromosome 22q11 deletion syndrome: An update and review for the primary pediatrician . Clin Pediatr1997;36:253-266.
4.
Bawle EV, Conrad J., Van Dyke DL, et al: Seven new cases of Cayler cardiofacial syndrome with chromosome 22q11.2 deletions, including a familial case. Am J Med Genet1998;79:406-410.
5.
Giannoti A., Digilio MC, Marino B., et al: Cayler cardiofacial syndrome and del 22q11: Part of CATCH 22 phenotype. Am J Med Genet1994;53:303-304.
6.
Rauch A., Hofbeck M., Bahring S., et al: Monozygotic twins concordant for Cayler syndrome. Am J Med Genet1998;75:113-117.
7.
Stewart HS, Clayton Smith J: Two patients with asymmetric crying facies, normal cardiovascular systems and deletion of chromosome 22q11. Clin Dysmorphol1997;6:165-169.
8.
Hopkin RJ, Schorry EK, Bofmger M., et al: Increased need for medical interventions in infants with velocardiofacial (deletion 22q11) syndrome. J Pediatr2000;137:247-249.
