Detalhe da pesquisa
1.
Isolated dentinogenesis imperfecta: Novel DSPP variants and insights on genetic counselling.
Clin Oral Investig
; 28(5): 254, 2024 Apr 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-38630328
2.
Genetic and Molecular Evaluation: Reporting Three Novel Mutations and Creating Awareness of Pycnodysostosis Disease.
Genes (Basel)
; 12(10)2021 09 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-34680947
3.
Gene Mutations of the Three Ectodysplasin Pathway Key Players (EDA, EDAR, and EDARADD) Account for More than 60% of Egyptian Ectodermal Dysplasia: A Report of Seven Novel Mutations.
Genes (Basel)
; 12(9)2021 09 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-34573371
4.
Further delineation of the oculoauricular syndrome phenotype: A new family with a novel truncating HMX1 mutation.
Ophthalmic Genet
; 39(2): 215-220, 2018 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29140751
5.
Generalised versus Regional Odontodysplasia: Diagnosis, Transitional Management, and Long-Term Followup-A Report of 2 Cases.
Case Rep Dent
; 2013: 519704, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23476815