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One Mutation of the ED1 Gene in a Chinese Han Family with X-Linked Hypohidrotic Ectodermal Dysplasia

Wang J, Ha WW, Wang W, Tang HY, Tang XF, Zheng XD, Zhu J, Yin XY, Yang S, Zhang XJ

No abstract available.
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A Novel Missense Mutation of Keratin 17 Gene in a Chinese Family with Steatocystoma Multiplex

Ha WW, Wang J, Wang W, Fu HY, Tang HY, Tang XF, Zhu J, Yin XY, Yang S, Zhang XJ

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Aspiration Pneumonia in Preterm Infants on Oral Feeds after Aspiration is Confirmed by VFSS: Case Series

Lee KW, Kim SB, Kang MG, Lee JH, Ha WW

Premature infants often face oral feeding problems. The videofluoroscopic swallow study (VFSS) is a commonly used method to detect subglottic aspiration. However, there is no consensus to date regarding the...
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