Mutational analysis for GJB2, GJB6, and GJB3 genes in Campania within a universal neonatal hearing screening programme.
about
Newborn hearing screening in the Campania region (Italy): early language and perceptual outcomes of infants with permanent hearing loss.Phenotypic and genetic characterization of a family carrying two Xq21.1-21.3 interstitial deletions associated with syndromic hearing loss.GJB2-associated hearing loss: systematic review of worldwide prevalence, genotype, and auditory phenotype.Distribution and phenotype of GJB2 mutations in 102 Sicilian patients with congenital non syndromic sensorineural hearing loss.
P2860
Mutational analysis for GJB2, GJB6, and GJB3 genes in Campania within a universal neonatal hearing screening programme.
description
2011 nî lūn-bûn
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2011年の論文
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2011年学术文章
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2011年学术文章
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2011年学术文章
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2011年学术文章
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name
Mutational analysis for GJB2, ...... l hearing screening programme.
@en
Mutational analysis for GJB2, ...... l hearing screening programme.
@nl
type
label
Mutational analysis for GJB2, ...... l hearing screening programme.
@en
Mutational analysis for GJB2, ...... l hearing screening programme.
@nl
prefLabel
Mutational analysis for GJB2, ...... l hearing screening programme.
@en
Mutational analysis for GJB2, ...... l hearing screening programme.
@nl
P2093
P2860
P1476
Mutational analysis for GJB2, ...... l hearing screening programme.
@en
P2093
Annamaria Franzè
Francesca De Falco
Gennaro Auletta
Giorgio Lilli
Maria De Luca
Pasquale Giannini
Pasquale Riccardi
Rita Malesci
Sandra Iossa
Virginia Corvino
P2860
P304
P356
10.3109/14992027.2011.603757
P577
2011-09-15T00:00:00Z