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Genetic Analysis of Hereditary Non-Syndromic Oral Clefts

NCT00340626 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 690

Last updated 2020-03-13

No results posted yet for this study

Summary

In a collaborative effort with the IBN AL-NAFEES Hospital (Damascus, Syrian Arab Republic), individuals from multiplex families determined to have hereditary oral clefts will be studied. The purpose of this study is to identify the gene(s) involved in heritable oral clefts by linkage analysis and gene mapping strategies. Characterization of genes involved in inherited oral clefts could provide important insight into the inheritance and pathogenesis of this disease.

Conditions

  • Hereditary Oral Clefts

Sponsors & Collaborators

  • National Human Genome Research Institute (NHGRI)

    lead NIH

Principal Investigators

  • Joan Bailey-Wilson, Ph.D. · National Human Genome Research Institute (NHGRI)

Eligibility

Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
1997-08-31
Primary Completion
2020-03-12
Completion
2020-03-12

Countries

  • Syria

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00340626 on ClinicalTrials.gov