Recurrent c.G1636A (p.G546S) mutation of COL2A1 in a Chinese family with skeletal dysplasia and different metaphyseal changes: a case report.
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Recurrent c.G1636A (p.G546S) mutation of COL2A1 in a Chinese family with skeletal dysplasia and different metaphyseal changes: a case report.
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2017 nî lūn-bûn
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2017年の論文
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2017年学术文章
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2017年学术文章
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2017年學術文章
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2017年學術文章
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Recurrent c.G1636A (p.G546S) m ...... hyseal changes: a case report.
@en
type
label
Recurrent c.G1636A (p.G546S) m ...... hyseal changes: a case report.
@en
prefLabel
Recurrent c.G1636A (p.G546S) m ...... hyseal changes: a case report.
@en
P2093
P2860
P1433
P1476
Recurrent c.G1636A (p.G546S) m ...... hyseal changes: a case report.
@en
P2093
P2860
P2888
P356
10.1186/S12887-017-0930-9
P577
2017-07-24T00:00:00Z
P6179
1090885708