Congenital sensorineural hearing loss as the initial presentation of PTPN11-associated Noonan syndrome with multiple lentigines or Noonan syndrome: clinical features and underlying mechanisms.

Congenital sensorineural hearing loss as the initial presentation of PTPN11-associated Noonan syndrome with multiple lentigines or Noonan syndrome: clinical features and underlying mechanisms.
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DOI:
10.1136/jmedgenet-2020-106892
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发表时间:
2020
期刊:
J Med Genet.
影响因子:
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通讯作者:
Yuan Yongyi
Yuan Yongyi
中科院分区:
--
文献类型:
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作者:
Gao Xue;Huang Shasha;Qiu Shiwei;Su Yu;Wang Weiqian;Xu Huiyan;Xu Jincao;Kang Dongyang;Dai Pu;Yuan Yongyi

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