Journal article
Genetics and genomics etiology of nonsyndromic orofacial clefts
Molecular genetics & genomic medicine, Vol.5(1), pp.3-7
01/2017
DOI: 10.1002/mgg3.272
PMCID: PMC5241211
PMID: 28116324
Abstract
Orofacial clefts (OFC) are complex birth defects. Studies using contemporary genomic techniques, bioinformatics, and statistical analyses have led to appreciable advances in identifying the causes of syndromic forms of clefts. This commentary gives an overview of the important cleft gene discoveries found using various genomic methods and tools.
Details
- Title: Subtitle
- Genetics and genomics etiology of nonsyndromic orofacial clefts
- Creators
- Wasiu L Adeyemo - Department of Oral and Maxillofacial Surgery College of Medicine University of Lagos Surulere NigeriaAzeez Butali - Department of Oral Pathology, Radiology and MedicineCollege of DentistryUniversity of IowaIowa CityIowa; Iowa Institute of Oral Health ResearchCollege of DentistryUniversity of IowaIowa CityIowa
- Resource Type
- Journal article
- Publication Details
- Molecular genetics & genomic medicine, Vol.5(1), pp.3-7
- DOI
- 10.1002/mgg3.272
- PMID
- 28116324
- PMCID
- PMC5241211
- NLM abbreviation
- Mol Genet Genomic Med
- ISSN
- 2324-9269
- eISSN
- 2324-9269
- Publisher
- United States
- Grant note
- DOI: 10.13039/100000867, name: Robert Wood Johnson Foundation, award: 72429
- Language
- English
- Date published
- 01/2017
- Academic Unit
- Oral Pathology, Radiology and Medicine; Stead Family Department of Pediatrics; Craniofacial Anomalies Research Center; Dental Research
- Record Identifier
- 9984065704702771
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