[Prenatal diagnosis of a novel SOX10 mutation in a patient with syndromic hearing loss].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 36(5): 477-479, 2019 May 10.
Article
in Zh
| MEDLINE
| ID: mdl-31030437
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Waardenburg Syndrome
/
SOXE Transcription Factors
/
Hearing Loss
Type of study:
Diagnostic_studies
Limits:
Female
/
Humans
/
Pregnancy
Language:
Zh
Journal:
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
Journal subject:
GENETICA MEDICA
Year:
2019
Document type:
Article
Country of publication:
China