Publications by authors named "Su-yan Yang"
Article Synopsis
- * A study analyzed genetic data from 2,901 sporadic Chinese NSHL patients, identifying 33 likely causative variants in 21 patients, including 20 novel variants which meet ACMG criteria.
- * The research indicates that variants in DFNB77 are relatively common among Chinese NSHL patients (0.72% of the studied population) and may aid in molecular diagnosis and genetic counseling for the condition.
Hereditary hearing loss is characterized by remarkable phenotypic heterogeneity. Patients with the same pathogenic mutations may exhibit various hearing loss phenotypes. In the Chinese population, the c.
View Article and Find Full Text PDFBackground: It is of high incidence of brain injuries in premature infants, so it is necessary to diagnose and treat the brain injury early for neonatal clinical practice. We are aimed to investigate the relationship between early postnatal cranial ultrasonography and psychomotor and mental development in prematrue infants at the age of 12 months.
Methods: Two-hundred and eight premature infants were selected and underwent follow-up from January, 2007 to November, 2012.