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G

Guillaume Captier

CHU de Montpellier
H指数:25
被引数:2,204

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POLR1B and neural crest cell anomalies in Treacher Collins syndrome type 4

Treacher Collins综合征4型的POLR1B和神经嵴细胞异常

2020-03-0162
OAAI
Postzygotic inactivating mutations of RHOA cause a mosaic neuroectodermal syndrome (vol 51, pg 1438, 2019)
2020-02-070
OAAI
Postzygotic inactivating mutations of RHOA cause a mosaic neuroectodermal syndrome (vol 51, pg 1438, 2019)
2019-10-142
OAAI
Postzygotic inactivating mutations of RHOA cause a mosaic neuroectodermal syndrome
2019-09-3025
OAAI
B3GAT3-related disorder with craniosynostosis and bone fragility due to a unique mutation
2018-02-0122
OAAI