P. Medeiros

Laryngeal atresia type III (glottic web) with 22q11.2 microdeletion: report of three patients.

S. Antonarakis, C. Stoll, A. Bottani, 1997, American journal of medical genetics.

De novo trisomy 22 due to an extra 22Q-chromosome.

C. Stoll, A. Schnebelen, H. Pécheur, 1997, Annales de genetique.

Johanson–Blizzard syndrome—A case study of oral and systemic manifestations

G. Godoy, P. Alves, Keila Martha Amorim Barroso, 2010 .

A Multicentric Brazilian Investigative Study of Copy Number Variations in Patients with Congenital Anomalies and Intellectual Disability

D. Bertola, R. Honjo, M. F. Galera, 2018, Scientific Reports.