Heterozygous deletion at the SOX10 gene locus in two patients from a Chinese family with Waardenburg syndrome type II. [electronic resource]
Producer: 20160426Description: 1718-21 p. digitalISSN:- 1872-8464
- Case-Control Studies
- China
- Chromosomes, Human, Pair 22
- Female
- Gene Deletion
- Gene Dosage
- Heterozygote
- Humans
- Infant
- Male
- Microphthalmia-Associated Transcription Factor -- genetics
- PAX3 Transcription Factor
- Paired Box Transcription Factors -- genetics
- Pedigree
- SOXE Transcription Factors -- genetics
- Waardenburg Syndrome -- genetics
- Young Adult
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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