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1.
Phenotype-genotype analysis of the autosomal recessive hereditary hearing loss caused by OTOA variations / 中华耳鼻咽喉头颈外科杂志
Chinese Journal of Otorhinolaryngology Head and Neck Surgery
; (12): 460-469, 2023.
Artículo
en Zh
| WPRIM | ID: wpr-986912
2.
Analysis of COL1A1 gene variation and clinical prevention and treatment in patients with Van der Hoeve syndrome / 中华耳鼻咽喉头颈外科杂志
Chinese Journal of Otorhinolaryngology Head and Neck Surgery
; (12): 1292-1299, 2021.
Artículo
en Zh
| WPRIM | ID: wpr-942615
3.
Preliminary audiological evaluation of the SoundBite bone conduction devices in adults with single-sided deafness / 中华耳鼻咽喉头颈外科杂志
Chinese Journal of Otorhinolaryngology Head and Neck Surgery
; (12): 478-486, 2021.
Artículo
en Zh
| WPRIM | ID: wpr-942463
4.
Primary tumors at the cervicothoracic junction / 中华耳鼻咽喉头颈外科杂志
Chinese Journal of Otorhinolaryngology Head and Neck Surgery
; (12): 922-925, 2012.
Artículo
en Zh
| WPRIM | ID: wpr-262444
5.
Prenatal genetic counseling and instruction for deaf families by genetic test / 中华耳鼻咽喉头颈外科杂志
Chinese Journal of Otorhinolaryngology Head and Neck Surgery
; (12): 909-913, 2011.
Artículo
en Zh
| WPRIM | ID: wpr-322438
6.
Sequence analysis of GJB3 in Chinese deafness population who carry one heterozygous GJB2 pathogenic mutation / 中华耳鼻咽喉头颈外科杂志
Chinese Journal of Otorhinolaryngology Head and Neck Surgery
; (12): 287-290, 2010.
Artículo
en Zh
| WPRIM | ID: wpr-276488
7.
Sequencing analysis of whole SLC26A4 gene in severe to profound sensorineural hearing loss patients with IVS7-2A to G mutation of the gene / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 610-615, 2010.
Artículo
en Zh
| WPRIM | ID: wpr-234353
8.
Real-time Taqman probe technique system for detecting the MtDNA 1555 A > G mutation / 中华耳鼻咽喉头颈外科杂志
Chinese Journal of Otorhinolaryngology Head and Neck Surgery
; (12): 160-164, 2009.
Artículo
en Zh
| WPRIM | ID: wpr-245937
9.
Sequencing analysis of whole SLC26A4 gene related to IVS7-2A > G mutation in 1552 moderate to profound sensorineural hearing loss patients in China / 中华耳鼻咽喉头颈外科杂志
Chinese Journal of Otorhinolaryngology Head and Neck Surgery
; (12): 449-454, 2009.
Artículo
en Zh
| WPRIM | ID: wpr-245905
10.
Etiologic analysis of severe to profound hearing loss patients from Chifeng city in Inner Mongolia / 中华耳鼻咽喉头颈外科杂志
Chinese Journal of Otorhinolaryngology Head and Neck Surgery
; (12): 292-296, 2009.
Artículo
en Zh
| WPRIM | ID: wpr-339215
11.
New surgical method for contact granuloma of larynx / 中华耳鼻咽喉头颈外科杂志
Chinese Journal of Otorhinolaryngology Head and Neck Surgery
; (12): 746-748, 2009.
Artículo
en Zh
| WPRIM | ID: wpr-317234
12.
Frequency of SLC26A4 IVS7-2A > G mutation in patients with severe to profound hearing loss from different area and ethnic group in China / 中华耳鼻咽喉头颈外科杂志
Chinese Journal of Otorhinolaryngology Head and Neck Surgery
; (12): 893-897, 2007.
Artículo
en Zh
| WPRIM | ID: wpr-309395
13.
Features of nationwide distribution and frequency of a common gap junction beta-2 gene mutation in China / 中华耳鼻咽喉头颈外科杂志
Chinese Journal of Otorhinolaryngology Head and Neck Surgery
; (12): 804-808, 2007.
Artículo
en Zh
| WPRIM | ID: wpr-309423
14.
Genetic counseling and instruction for deaf couples directed by genetic testing / 中华耳鼻咽喉头颈外科杂志
Chinese Journal of Otorhinolaryngology Head and Neck Surgery
; (12): 499-503, 2007.
Artículo
en Zh
| WPRIM | ID: wpr-270784
15.
Patients suffered from enlarged vestibular aqueduct syndrome in Chifeng deaf and dumb school detected by Pendred's syndrome gene hot spot mutation screening / 中华耳鼻咽喉头颈外科杂志
Chinese Journal of Otorhinolaryngology Head and Neck Surgery
; (12): 497-500, 2006.
Artículo
en Zh
| WPRIM | ID: wpr-298835
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