Whole-exome sequencing to identify the cause of congenital sensorineural hearing loss in carriers of a heterozygous GJB2 mutation.
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Whole-exome sequencing to identify the cause of congenital sensorineural hearing loss in carriers of a heterozygous GJB2 mutation.
description
2017 nî lūn-bûn
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2017年の論文
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2017年論文
@yue
2017年論文
@zh-hant
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@zh-hk
2017年論文
@zh-mo
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@zh-tw
2017年论文
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name
Whole-exome sequencing to iden ...... a heterozygous GJB2 mutation.
@en
type
label
Whole-exome sequencing to iden ...... a heterozygous GJB2 mutation.
@en
prefLabel
Whole-exome sequencing to iden ...... a heterozygous GJB2 mutation.
@en
P2093
P2860
P50
P1476
Whole-exome sequencing to iden ...... a heterozygous GJB2 mutation.
@en
P2093
Alexandra Frohne
Andreas Kirchnawy
Berthold Streubel
Klemens Frei
Martin Koenighofer
P2860
P2888
P356
10.1007/S00405-017-4699-0
P577
2017-08-18T00:00:00Z