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Literature DB >> 10979110

Genetic testing to identify deaf newborns.

G E Green, R J Smith, J P Bent, E S Cohn.

Abstract

Mesh：

Substances：
Connexins
Connexin 26

Year: 2000 PMID： 10979110 DOI： 10.1001/jama.284.10.1245

Source DB: PubMed Journal: JAMA ISSN： 0098-7484 Impact factor: 56.272

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6 in total

1. Concurrent Hearing and Genetic Screening of 180,469 Neonates with Follow-up in Beijing, China.

Authors: Pu Dai; Li-Hui Huang; Guo-Jian Wang; Xue Gao; Chun-Yan Qu; Xiao-Wei Chen; Fu-Rong Ma; Jie Zhang; Wan-Li Xing; Shu-Yan Xi; Bin-Rong Ma; Ying Pan; Xiao-Hua Cheng; Hong Duan; Yong-Yi Yuan; Li-Ping Zhao; Liang Chang; Ru-Zhen Gao; Hai-Hong Liu; Wei Zhang; Sha-Sha Huang; Dong-Yang Kang; Wei Liang; Ke Zhang; Hong Jiang; Yong-Li Guo; Yi Zhou; Wan-Xia Zhang; Fan Lyu; Ying-Nan Jin; Zhen Zhou; Hong-Li Lu; Xin Zhang; Ping Liu; Jia Ke; Jin-Sheng Hao; Hai-Meng Huang; Di Jiang; Xin Ni; Mo Long; Luo Zhang; Jie Qiao; Cynthia Casson Morton; Xue-Zhong Liu; Jing Cheng; De-Min Han
Journal: Am J Hum Genet Date: 2019-09-26 Impact factor: 11.025

Genetic testing to identify deaf newborns.

1. Concurrent Hearing and Genetic Screening of 180,469 Neonates with Follow-up in Beijing, China.

Review 2. Hereditary non-syndromic sensorineural hearing loss: transforming silence to sound.

3. Audiologic phenotype and progression in GJB2 (Connexin 26) hearing loss.

4. Residual Hearing in DFNB1 Deafness and Its Clinical Implication in a Korean Population.

Review 5. DFNB1 Non-syndromic Hearing Impairment: Diversity of Mutations and Associated Phenotypes.

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