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1.
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
2.
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
3.
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
4.
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
5.
Preliminary study on the functional localization of auditory cortex in auditory pathology patients using magnetoencephalography / 中华耳鼻咽喉头颈外科杂志
Chinese Journal of Otorhinolaryngology Head and Neck Surgery
; (12): 346-350, 2006.
Artículo
en Zh
| WPRIM | ID: wpr-308901
6.
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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