Found: 19
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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
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- Article
Clinically actionable secondary findings in 130 triads from sub‐Saharan African families with non‐syndromic orofacial clefts.
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- Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 10, p. 1, doi. 10.1002/mgg3.2237
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- Article
Novel IRF6 variant in orofacial cleft patients from Durban, South Africa.
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- Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 5, p. 1, doi. 10.1002/mgg3.2138
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- Article
Co‐occurrence of orofacial clefts and clubfoot phenotypes in a sub‐Saharan African cohort: Whole‐exome sequencing implicates multiple syndromes and genes.
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- Molecular Genetics & Genomic Medicine, 2021, v. 9, n. 4, p. 1, doi. 10.1002/mgg3.1655
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- Article
Non‐random distribution of deleterious mutations in the DNA and protein‐binding domains of IRF6 are associated with Van Der Woude syndrome.
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- Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 8, p. 1, doi. 10.1002/mgg3.1355
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- Article
A mutational hotspot in AMOTL1 defines a new syndrome of orofacial clefting, cardiac anomalies, and tall stature.
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- American Journal of Medical Genetics. Part A, 2023, v. 191, n. 5, p. 1227, doi. 10.1002/ajmg.a.63130
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- Article
Perceptions and beliefs of community gatekeepers about genomic risk information in African cleft research.
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- BMC Public Health, 2024, v. 24, n. 1, p. 1, doi. 10.1186/s12889-024-17987-z
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- Article
Damaging Mutations in AFDN Contribute to Risk of Nonsyndromic Cleft Lip With or Without Cleft Palate.
- Published in:
- Cleft Palate Craniofacial Journal, 2024, v. 61, n. 4, p. 697, doi. 10.1177/10556656221135926
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- Article
Novel GRHL3 Variants in a South African Cohort With Cleft Lip and Palate.
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- Cleft Palate Craniofacial Journal, 2022, v. 59, n. 9, p. 1125, doi. 10.1177/10556656211038453
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- Article
Genome-Wide Scan for Parent-of-Origin Effects in a sub-Saharan African Cohort With Nonsyndromic Cleft Lip and/or Cleft Palate (CL/P).
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- Cleft Palate Craniofacial Journal, 2022, v. 59, n. 7, p. 841, doi. 10.1177/10556656211036316
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- Article
Genetic heterogeneity and enrichment of variants in DNA‐repair genes in ameloblastoma.
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- Journal of Oral Pathology & Medicine, 2023, v. 52, n. 3, p. 263, doi. 10.1111/jop.13410
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- Article
Variant Analyses of Candidate Genes in Orofacial Clefts in Multi‐Ethnic Populations.
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- FASEB Journal, 2021, v. 35, p. N.PAG, doi. 10.1096/fasebj.2021.35.S1.03614
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- Article
Role of Rare Variants in Craniofacial Enhancer Regions in the Etiology of Non‐Syndromic Orofacial Clefts.
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- FASEB Journal, 2021, v. 35, p. N.PAG, doi. 10.1096/fasebj.2021.35.S1.04371
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- Article
Periconceptional use of vitamin A and the risk of giving birth to a child with nonsyndromic orofacial clefts—A meta‐analysis.
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- Birth Defects Research, 2022, v. 114, n. 10, p. 467, doi. 10.1002/bdr2.2005
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- Article
Variant analyses of candidate genes in orofacial clefts in multi‐ethnic populations.
- Published in:
- Oral Diseases, 2022, v. 28, n. 7, p. 1921, doi. 10.1111/odi.13932
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- Article
Genetic and epigenetic studies in non‐syndromic oral clefts.
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- Oral Diseases, 2022, v. 28, n. 5, p. 1339, doi. 10.1111/odi.14146
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- Article
Replication of GWAS significant loci in a sub-Saharan African Cohort with early childhood caries: a pilot study.
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- BMC Oral Health, 2021, v. 21, n. 1, p. 1, doi. 10.1186/s12903-021-01623-y
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- Article
Shared genetic risk between major orofacial cleft phenotypes in an African population.
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- Genetic Epidemiology, 2024, v. 48, n. 6, p. 258, doi. 10.1002/gepi.22564
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- Article
Baseline assessment of oral health needs among underserved populations in the United States.
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- Journal of Global Oral Health, 2023, v. 6, n. 1, p. 38, doi. 10.25259/JGOH_3_2023
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- Article