11 results on '"Huang, Lihui"'
Search Results
2. Mutation analysis of the SLC26A4 gene in three Chinese families
3. Analysis of mutations in the FOXI1 and KCNJ10 genes in infants with a single-allele SLC26A4 mutation
4. Novel compound heterozygous mutations in SLC26A4 gene in a Chinese family with enlarged vestibular aqueduct
5. Children with GJB2 gene mutations have various audiological phenotypes
6. Clinical data analysis of genotypes and phenotypes of deafness gene mutations in newborns: A retrospective study
7. Analysis of p.V37I compound heterozygous mutations in the GJB2 gene in Chinese infants and young children
8. Genetic screening of newborns for deafness over 11 years in Beijing, China: More infants could benefit from an expanded program.
9. High-frequency hearing vulnerability associated with the different supporting potential of Hensen's cells: SMART-Seq2 RNA sequencing.
10. 2008 Beijing Symposium on a Hearing Screening Program for Neonates and Children: Perspectives on interdisciplinary and international collaboration.
11. Audiological characteristics of infants with abnormal transient evoked otoacoustic emission and normal auditory brainstem response.
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