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

about

Antibiotic-induced release of small extracellular vesicles (exosomes) with surface-associated DNA.Large scale newborn deafness genetic screening of 142,417 neonates in Wuhan, China.Polymorphism of the 86th amino acid in CX26 protein and hereditary deafness.

P2860

Q40091997-FD9551DF-3E80-4EA2-B5F0-185DDFAC0B37 Q55189646-EB663C41-DA78-4908-A92D-76514D3221D1 Q55248663-D25DAFA4-9D13-4221-AB8C-F5B1E7954EE5

P2860

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

Item

http://www.wikidata.org/entity/Q42072188

description

2015 nî lūn-bûn

@nan

2015年の論文

@ja

2015年学术文章

@wuu

2015年学术文章

@zh-cn

2015年学术文章

@zh-hans

2015年学术文章

@zh-my

2015年学术文章

@zh-sg

2015年學術文章

@yue

2015年學術文章

@zh

2015年學術文章

@zh-hant

name

Cordblood-Based High-Throughpu ...... wborns in Jinan Area of China.

@en

Cordblood-Based High-Throughpu ...... wborns in Jinan Area of China.

@nl

type

Item

label

Cordblood-Based High-Throughpu ...... wborns in Jinan Area of China.

@en

Cordblood-Based High-Throughpu ...... wborns in Jinan Area of China.

@nl

prefLabel

Cordblood-Based High-Throughpu ...... wborns in Jinan Area of China.

@en

Cordblood-Based High-Throughpu ...... wborns in Jinan Area of China.

@nl

P1476

Cordblood-Based High-Throughpu ...... wborns in Jinan Area of China.

@en

P2093

Cai-Xia Sun

http://www.w3.org/2001/XMLSchema#string

Ding-Li Chen

http://www.w3.org/2001/XMLSchema#string

Gen-Dong Yao

http://www.w3.org/2001/XMLSchema#string

Hai-Qin Feng

http://www.w3.org/2001/XMLSchema#string

Li-Li Guo

http://www.w3.org/2001/XMLSchema#string

Li-Li Ping

http://www.w3.org/2001/XMLSchema#string

Shou-Xia Li

http://www.w3.org/2001/XMLSchema#string

Su-Bin Zhao

http://www.w3.org/2001/XMLSchema#string

Xiao-Fang Zhang

http://www.w3.org/2001/XMLSchema#string

Zhi-Ming Yang

http://www.w3.org/2001/XMLSchema#string

P2860

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

Newborn genetic screening for hearing impairment: a preliminary study at a tertiary center

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

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

GJB2 mutations and degree of hearing loss: a multicenter study.

Common molecular etiologies are rare in nonsyndromic Tibetan Chinese patients with hearing impairment.

The p.V37I exclusive genotype of GJB2: a genetic risk-indicator of postnatal permanent childhood hearing impairment.

Universal neonatal hearing screening moving from evidence to practice

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

The genetic bases for non-syndromic hearing loss among Chinese

P304

211-217

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.3342/CEO.2015.8.3.211

http://www.w3.org/2001/XMLSchema#string

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P577

2015-08-13T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

281541810

http://www.w3.org/2001/XMLSchema#string

P698

26330914

http://www.w3.org/2001/XMLSchema#string

P932

4553350

http://www.w3.org/2001/XMLSchema#string

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

about

P2860

P2860

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

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P5875

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P5875

P698

P932