Mutation in the X-linked RAB40AL gene (Martin-Probst syndrome) with mental retardation, sensorineural hearing loss, and anomalies of the craniofacies and genitourinary tract: a second case report.
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Mutation in the X-linked RAB40AL gene (Martin-Probst syndrome) with mental retardation, sensorineural hearing loss, and anomalies of the craniofacies and genitourinary tract: a second case report.
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2014 nî lūn-bûn
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2014年の論文
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2014年学术文章
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2014年学术文章
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2014年学术文章
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2014年学术文章
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2014年学术文章
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name
Mutation in the X-linked RAB40 ...... y tract: a second case report.
@en
Mutation in the X-linked RAB40 ...... y tract: a second case report.
@nl
type
label
Mutation in the X-linked RAB40 ...... y tract: a second case report.
@en
Mutation in the X-linked RAB40 ...... y tract: a second case report.
@nl
prefLabel
Mutation in the X-linked RAB40 ...... y tract: a second case report.
@en
Mutation in the X-linked RAB40 ...... y tract: a second case report.
@nl
P2860
P1476
Mutation in the X-linked RAB40 ...... y tract: a second case report.
@en
P2093
Richard G Boles
Stacey Wong
P2860
P2888
P304
P356
10.1007/S00431-014-2339-X
P50
P577
2014-05-27T00:00:00Z