Pages that link to "Q33312492"

The following pages link to Construction of a multiplex allele-specific PCR-based universal array (ASPUA) and its application to hearing loss screening (Q33312492):

Displaying 22 items.

• The future role of genetic screening to detect newborns at risk of childhood-onset hearing loss (Q26863583) (← links)
• An automated microfluidic system for single-stranded DNA preparation and magnetic bead-based microarray analysis. (Q27331965) (← links)
• Genetic frequencies related to severe or profound sensorineural hearing loss in Inner Mongolia Autonomous Region (Q30368252) (← links)
• Rapid and Reliable Detection of Nonsyndromic Hearing Loss Mutations by Multicolor Melting Curve Analysis (Q30839526) (← links)
• Targeted genomic capture and massively parallel sequencing to identify novel variants causing Chinese hereditary hearing loss (Q34527976) (← links)
• The carrier rate and mutation spectrum of genes associated with hearing loss in South China hearing female population of childbearing age. (Q34746920) (← links)
• Impact of gene patents and licensing practices on access to genetic testing for hearing loss (Q35073561) (← links)
• Genetic mutations in non-syndromic deafness patients of Uyghur and Han Chinese ethnicities in Xinjiang, China: a comparative study (Q35289974) (← links)
• Screening of deafness-causing DNA variants that are common in patients of European ancestry using a microarray-based approach (Q36300634) (← links)
• Mitochondrial COX2 G7598A mutation may have a modifying role in the phenotypic manifestation of aminoglycoside antibiotic-induced deafness associated with 12S rRNA A1555G mutation in a Han Chinese pedigree (Q36553950) (← links)
• GJB2 mutation spectrum in 2,063 Chinese patients with nonsyndromic hearing impairment (Q37185905) (← links)
• A novel compound heterozygous mutation in the GJB2 gene causing non-syndromic hearing loss in a family (Q37496120) (← links)
• Genetic diagnosis and cochlear implantation for patients with nonsyndromic hearing loss and enlarged vestibular aqueduct (Q37979920) (← links)
• One-step noninvasive prenatal testing (NIPT) for autosomal recessive homozygous point mutations using digital PCR. (Q50025522) (← links)
• A rapid automatic processing platform for bead label-assisted microarray analysis: application for genetic hearing-loss mutation detection. (Q50356655) (← links)
• Maternally transmitted aminoglycoside-induced and non-syndromic hearing loss caused by the 1494C > T mutation in the mitochondrial 12S rRNA gene in two Chinese families (Q50357935) (← links)
• A universal multiplex PCR strategy for 100-plex amplification using a hydrophobically patterned microarray (Q51546028) (← links)
• A Novel GJB2 compound heterozygous mutation c.257C>G (p.T86R)/c.176del16 (p.G59A fs*18) causes sensorineural hearing loss in a Chinese family. (Q52582883) (← links)
• A screening analysis of the GJB2 c.176 del 16 mutation responsible for hereditary deafness in a Chinese family. (Q55266022) (← links)
• Non-Syndromic Hearing Loss and High-Throughput Strategies to Decipher Its Genetic Heterogeneity (Q60307553) (← links)
• A dominant variant in the PDE1C gene is associated with nonsyndromic hearing loss (Q88962073) (← links)
• Concurrent Hearing and Genetic Screening of 180,469 Neonates with Follow-up in Beijing, China (Q90351381) (← links)