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Your search keyword '"Yuan, Hui Jun"' showing total 110 results

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110 results on '"Yuan, Hui Jun"'

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1. Disease-specific ACMG/AMP guidelines improve sequence variant interpretation for hearing loss

3. ClinGen expert clinical validity curation of 164 hearing loss gene–disease pairs

17. Correction: ClinGen expert clinical validity curation of 164 hearing loss gene–disease pairs

18. ZxNHX1 indirectly participates in controlling K+ homeostasis in the xerophyte Zygophyllum xanthoxylum.

20. GJB2 mutation spectrum in Inner Mongolia and its comparison with other Asian populations

21. GJB2 mutation spectrum in deaf population in a typical southeastern area of China

23. License plate recognition based on mathematical morphology method and RBF neural network

26. ZxAKT1 is essential for K+ uptake and K+/Na+ homeostasis in the succulent xerophyte Zygophyllum xanthoxylum.

36. Hearing loss and PRPS1 mutations: Wide spectrum of phenotypes and potential therapy.

37. Mitochondrial DNA A1555G mutation screening using a testing kit method and its significance in preventing aminoglycoside-related hearing loss

38. Advancements and prospects in reconstructing the genetic genealogies of ancient and modern human populations using ancestral recombination graphs.

39. [Prediction of quality markers of Angong Niuhuang Pills based on LC-MS and pull-down with SPR chips].

40. ZxNHX1 indirectly participates in controlling K + homeostasis in the xerophyte Zygophyllum xanthoxylum.

41. [Simultaneous determination of seven bioactive compounds and pharmacokinetics in rat plasma after oral administration of Yindan Xinnaotong Ruanjiaonang by UPLC-MS/MS].

42. ZxAKT1 is essential for K + uptake and K + /Na + homeostasis in the succulent xerophyte Zygophyllum xanthoxylum.

43. Application and progress of high-throughput sequencing technologies in the research of hereditary hearing loss.

45. [Clinical features and screening of ACVRL1 gene in II hereditary hemorrhagic telangiectasia].

46. [Detection of trisomy 21 by quantitative fluorescent PCR in clinical samples undergoing prenatal diagnosis for hereditary hearing loss].

47. [Study on the association between IL-2R and IL-7R gene polymorphism and idiopathic demyelinating optic neuritis].

48. [Development of multiple quantitative fluorescent PCR for rapid diagnosis of common aneuploidy and it's clinical application].

49. [Study on the chemical constituents from Clematis brevicaudata].

50. [Molecular etiology of non-syndromic hearing impairment in a Chinese family].

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