Detalhe da pesquisa
1.
Genomic analyses in African populations identify novel risk loci for cleft palate.
Hum Mol Genet
; 28(6): 1038-1051, 2019 03 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-30452639
2.
A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3.
Am J Hum Genet
; 98(4): 744-54, 2016 Apr 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-27018472
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.
Novel GREM1 Variations in Sub-Saharan African Patients With Cleft Lip and/or Cleft Palate.
Cleft Palate Craniofac J
; 55(5): 736-742, 2018 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29489415
5.
Whole-genome sequencing reveals de-novo mutations associated with nonsyndromic cleft lip/palate.
Sci Rep
; 12(1): 11743, 2022 07 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-35817949
6.
Identification of paternal uniparental disomy on chromosome 22 and a de novo deletion on chromosome 18 in individuals with orofacial clefts.
Mol Genet Genomic Med
; 6(6): 924-932, 2018 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-30141273
7.
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