Detalhe da pesquisa
1.
WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes.
Am J Hum Genet
; 85(1): 97-105, 2009 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-19559398
2.
Deletions of the RUNX2 gene are present in about 10% of individuals with cleidocranial dysplasia.
Hum Mutat
; 31(8): E1587-93, 2010 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-20648631
3.
Development of a Rapid Analysis Method for Bone Resection Margins for Oral Squamous Cell Carcinoma by Immunoblotting.
Head Neck Pathol
; 12(2): 210-220, 2018 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-28929330