Detalhe da pesquisa
1.
Hearing loss and history of otolaryngological conditions in adults with microdeletion 22q11.2.
Am J Med Genet A
; 194(3): e63456, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-37916923
2.
A candidate gene approach to identify modifiers of the palatal phenotype in 22q11.2 deletion syndrome patients.
Int J Pediatr Otorhinolaryngol
; 77(1): 123-7, 2013 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-23121717
3.
Histology of the pharyngeal constrictor muscle in 22q11.2 deletion syndrome and non-syndromic children with velopharyngeal insufficiency.
PLoS One
; 6(6): e21672, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-21738760
4.
Outcome of velopharyngoplasty in patients with velocardiofacial syndrome.
Arch Otolaryngol Head Neck Surg
; 134(11): 1159-64, 2008 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-19015444