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常染色體隱性遺傳性非綜合征型耳聾
常染色體隱性遺傳性非綜合征型耳聾
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常染色體隱性遺傳性非綜合征型耳聾
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基因心片海鵬奏
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2023-10-09 10:06
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GJB2基因 c.235delC對應(yīng)哪個rs點位？
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冷靜的MYT1L基因
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2021-01-15 09:54
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我攜帶多個風(fēng)險突變耳聾？意味著什么？
蓄須的CFTR基因
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zhengqiang
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2019-02-20 13:34
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常染色體隱性遺傳性非綜合征型耳聾 攜帶 1 個風(fēng)險突變
努力的ABCC1基因
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微胖的EYS基因
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2019-02-19 19:31
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報告當(dāng)中沒有寫具體哪個位點變異
獼猴桃含有
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2019-01-18 00:16
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常染色體隱性遺傳性非綜合征型耳聾
5 個討論
相關(guān)基因
GJB2
位點：RS104894395
位點：RS104894409
位點：RS111033190
位點：RS111033203
位點：RS111033217
位點：RS111033294
位點：RS111033420
位點：RS111033451
位點：RS1801002
位點：RS28931592
位點：RS28931595
位點：RS80338949
位點：RS727504302
位點：RS772264564
位點：RS773528125
位點：RS781534323
SLC26A4
位點：RS111033318
位點：RS121908363
位點：RS200455203
OTOF
位點：RS111033330
位點：RS111033341
位點：RS111033342
位點：RS111033373
位點：RS111033383
位點：RS111033447
位點：RS143939430
位點：RS368790049
位點：RS370609551
位點：RS397515582
位點：RS397515584
位點：RS397515586
位點：RS397515605
位點：RS397515608
位點：RS80356584
位點：RS80356589
位點：RS80356597
位點：RS80356599
位點：RS80356604
位點：RS111033349
位點：RS200147906
位點：RS370132645
位點：RS727504936
MARVELD2
位點：RS118203957
TMC1
位點：RS121908073
位點：RS121908074
位點：RS151001642
位點：RS370088722
位點：RS367924428
位點：RS138527651
位點：RS730880359
ESRRB
位點：RS121909110
位點：RS121909111
位點：RS727503041
USH1C
位點：RS146451547
MYO3A
位點：RS193919333
位點：RS199541460
TMIE
位點：RS267607120
位點：RS28941781
位點：RS28942096
位點：RS28942097
位點：RS397517865
位點：RS397517866
MYO7A
位點：RS387906700
PNPT1
位點：RS397514599
MYO15A
位點：RS397517286
位點：RS375290498
位點：RS397517285
位點：RS377015931
位點：RS546575046
CDH23
位點：RS763721044
COL11A2
位點：RS606231410
COL4A4
位點：RS142093416
LOXHD1
位點：RS373937326
位點：RS727505104
MET
位點：RS794728016
MYO6
位點：RS727503326
OTOA
位點：RS148690740
STRC
位點：RS2920791
位點：RS199839039
TRIOBP
位點：RS370737996
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness.
A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness.
A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness.
A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness.
A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness.
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness.
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function.
Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function.
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness.
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function.
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
From flies' eyes to our ears: mutations in a human class III myosin cause progressive nonsyndromic hearing loss DFNB31
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness.
Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function.
A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness.
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness.
A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness.
A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness.
A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness.
A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness.
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness.
A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness.
A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness.
A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness.
A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness.
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23.
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
From flies' eyes to our ears: mutations in a human class III myosin cause progressive nonsyndromic hearing loss DFNB30.
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness.
A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness.
A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness.
A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness.
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function.
Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function.
Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function.
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
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深圳市市場監(jiān)督管理局企業(yè)主體身份公示
|
粵ICP備15012185號
|
互聯(lián)網(wǎng)藥品信息服務(wù)資格證書:（粵）-非經(jīng)營性-2023-0379
中文 
English
純合片段分析
姓氏祖源
祖源平均臉
基因關(guān)系
基因保險助手
原始數(shù)據(jù)
