Found: 9
Select item for more details and to access through your institution.
Whole-genome sequencing reveals de-novo mutations associated with nonsyndromic cleft lip/palate.
- Published in:
- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-15885-1
- By:
- Publication type:
- Article
Rare functional variants in genome-wide association identified candidate genes for nonsyndromic clefts in the African population.
- Published in:
- American Journal of Medical Genetics. Part A, 2014, v. 164A, n. 10, p. 2567, doi. 10.1002/ajmg.a.36691
- By:
- Publication type:
- Article
Novel GREM1 Variations in Sub-Saharan African Patients With Cleft Lip and/or Cleft Palate.
- Published in:
- Cleft Palate Craniofacial Journal, 2018, v. 55, n. 5, p. 736, doi. 10.1177/1055665618754948
- By:
- Publication type:
- Article
Oral health related quality of life (OHRQoL) following third molar surgery in Sub-Saharan Africans: an observational study.
- Published in:
- Pan African Medical Journal, 2016, v. 25, p. 1, doi. 10.11604/pamj.2016.25.97.7656
- By:
- Publication type:
- Article
Multidisciplinary approach to genomics research in Africa: the AfriCRAN model.
- Published in:
- Pan African Medical Journal, 2015, v. 21, p. 1, doi. 10.11604/pamj.2015.21.229.7380
- By:
- Publication type:
- Article
Pathologies Associated with Impacted Mandibular Third Molars in Sub-Saharan Africans.
- Published in:
- Dentistry & Medical Research, 2018, v. 6, n. 1, p. 2, doi. 10.4103/dmr.dmr_20_17
- By:
- Publication type:
- Article
Identification of paternal uniparental disomy on chromosome 22 and a de novo deletion on chromosome 18 in individuals with orofacial clefts.
- Published in:
- Molecular Genetics & Genomic Medicine, 2018, v. 6, n. 6, p. 924, doi. 10.1002/mgg3.459
- By:
- Publication type:
- Article
The prevalence, penetrance, and expressivity of etiologic IRF6 variants in orofacial clefts patients from sub-Saharan Africa.
- Published in:
- Molecular Genetics & Genomic Medicine, 2017, v. 5, n. 2, p. 164, doi. 10.1002/mgg3.273
- By:
- Publication type:
- Article
Novel IRF6 mutations in families with Van Der Woude syndrome and popliteal pterygium syndrome from sub-Saharan Africa.
- Published in:
- Molecular Genetics & Genomic Medicine, 2014, v. 2, n. 3, p. 254, doi. 10.1002/mgg3.66
- By:
- Publication type:
- Article