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Identification of Novel Mutations in Polydactyly Patients with Whole-Exome Sequencing

Identification of Novel Mutations in Polydactyly Patients with Whole-Exome Sequencing

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900021080
Enrollment
Unknown
Registered
2019-01-27
Start date
2017-10-01
Completion date
Unknown
Last updated
2019-01-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Polydactyly

Interventions

polydactyly:none

Sponsors

The First Hospital of Jilin University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: polydactyly without other disease

Exclusion criteria

Exclusion criteria: 1. family heredity; 2. fingers other than thumb

Design outcomes

Primary

MeasureTime frame
mutant gene;—

Countries

China

Contacts

Public ContactWang Tao

The First Hospital of Jilin University

w-t585@163.com+86 13944111303

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026