Cordblood-Based High-Throughput Screening for Deafness Gene of 646 Newborns in Jinan Area of China (Q42072188)

16 October 2017

Cordblood-Based High-Throughput Screening for Deafness Gene of 646 Newborns in Jinan Area of China (English)

1 reference

16 October 2017

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Shou-Xia Li

1

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16 October 2017

Ding-Li Chen

2

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16 October 2017

Su-Bin Zhao

3

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16 October 2017

Li-Li Guo

4

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16 October 2017

Hai-Qin Feng

5

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16 October 2017

Xiao-Fang Zhang

6

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16 October 2017

Li-Li Ping

7

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16 October 2017

Zhi-Ming Yang

8

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16 October 2017

Cai-Xia Sun

9

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16 October 2017

Gen-Dong Yao

10

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16 October 2017

13 August 2015

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Clinical and Experimental Otorhinolaryngology

16 October 2017

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16 October 2017

8

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16 October 2017

3

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16 October 2017

211-217

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Creative Commons Attribution-NonCommercial 3.0 Unported

16 October 2017

start time

1 January 2015

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

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Mitochondrial 12S rRNA variants in 1642 Han Chinese pediatric subjects with aminoglycoside-induced and nonsyndromic hearing loss

5 June 2018

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Mitochondrial haplotypes may modulate the phenotypic manifestation of the deafness-associated 12S rRNA 1555A>G mutation

5 June 2018

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Hypo-functional SLC26A4 variants associated with nonsyndromic hearing loss and enlargement of the vestibular aqueduct: genotype-phenotype correlation or coincidental polymorphisms?

5 June 2018

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The genetic bases for non-syndromic hearing loss among Chinese

5 June 2018

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GJB2 mutations and degree of hearing loss: a multicenter study

5 June 2018

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Universal neonatal hearing screening moving from evidence to practice

5 June 2018

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Maternally inherited aminoglycoside-induced and nonsyndromic deafness is associated with the novel C1494T mutation in the mitochondrial 12S rRNA gene in a large Chinese family

5 June 2018

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Origins and frequencies of SLC26A4 (PDS) mutations in east and south Asians: global implications for the epidemiology of deafness

5 June 2018

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Enlarged vestibular aqueduct: a radiological marker of pendred syndrome, and mutation of the PDS gene

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Evaluation of the pathogenicity of GJB3 and GJB6 variants associated with nonsyndromic hearing loss

5 June 2018

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Newborn hearing screening and genetic testing in 8974 Brazilian neonates

17 August 2018

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Infant hearing loss and connexin testing in a diverse population

17 August 2018

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A distinct spectrum of SLC26A4 mutations in patients with enlarged vestibular aqueduct in China

17 August 2018

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Does universal newborn hearing screening identify all children with GJB2 (Connexin 26) deafness? Penetrance of GJB2 deafness

17 August 2018

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A multicenter evaluation of how many infants with permanent hearing loss pass a two-stage otoacoustic emissions/automated auditory brainstem response newborn hearing screening protocol

17 August 2018

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Ethnicity and mutations in GJB2 (connexin 26) and GJB6 (connexin 30) in a multi-cultural Canadian paediatric Cochlear Implant Program.

17 August 2018

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SLC26A4/PDS genotype-phenotype correlation in hearing loss with enlargement of the vestibular aqueduct (EVA): evidence that Pendred syndrome and non-syndromic EVA are distinct clinical and genetic entities

17 August 2018

1 reference

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Language of early- and later-identified children with hearing loss

17 August 2018

1 reference

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Connexin 26 R143W mutation associated with recessive nonsyndromic sensorineural deafness in Africa

17 August 2018

1 reference

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17 August 2018

Mitochondrial deafness

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26330914

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

M34T and V37I mutations inGJB2 associated hearing impairment: Evidence for pathogenicity and reduced penetrance

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26330914

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.3342/CEO.2015.8.3.211

1 reference

16 October 2017

1 reference

16 October 2017

PubMed publication ID

26330914

1 reference