Detalhe da pesquisa
1.
Mutations in Van Der Woude Families From Ethiopia.
J Craniofac Surg
; 33(2): e138-e140, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-34643600
2.
The Role of Environmental Factors in the Etiology of Nonsyndromic Orofacial Clefts.
J Craniofac Surg
; 31(1): 113-116, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-31821209
3.
A multi-ethnic genome-wide association study identifies novel loci for non-syndromic cleft lip with or without cleft palate on 2p24.2, 17q23 and 19q13.
Hum Mol Genet
; 25(13): 2862-2872, 2016 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27033726
4.
Oral Health-Related Quality of Life of Children Born With Orofacial Clefts in Ethiopia and Their Parents.
Cleft Palate Craniofac J
; : 1055665618760619, 2018 Jan 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29561719
5.
Descriptive Epidemiology of Orofacial Clefts in Ethiopia.
J Craniofac Surg
; 28(2): 334-337, 2017 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-27984437
6.
Rare functional variants in genome-wide association identified candidate genes for nonsyndromic clefts in the African population.
Am J Med Genet A
; 164A(10): 2567-71, 2014 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-25081408
7.
Assessing the Practice of Birth Defect Registration at Addis Ababa Health Facilities.
Ethiop J Health Sci
; 31(3): 683-687, 2021 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-34483626
8.
The prevalence, penetrance, and expressivity of etiologic IRF6 variants in orofacial clefts patients from sub-Saharan Africa.
Mol Genet Genomic Med
; 5(2): 164-171, 2017 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-28361103
9.
Congenital Palatal Fistula Associated with Submucous Cleft Palate.
Plast Reconstr Surg Glob Open
; 4(2): e613, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-27014542
10.
Foreign Bodies Simulating a Congenital Palatal Fistula and Vascular Anomaly.
Case Rep Dent
; 2015: 387092, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26075109
11.
Novel IRF6 mutations in families with Van Der Woude syndrome and popliteal pterygium syndrome from sub-Saharan Africa.
Mol Genet Genomic Med
; 2(3): 254-60, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24936515