Suchergebnisse - "YUAN HUIJUN"

PubPharm (85)

1

Pseudoaneurysm of the internal iliac artery caused by proximal femoral nail antirotation following intertrochanteric fracture : a case report

enthalten in: The Journal of international medical research | 2019

von Ren, C. | Wang, Q. | Ma, T. | +5

2

Consensus interpretation of the p.Met34Thr and p.Val37Ile variants in GJB2 by the ClinGen Hearing Loss Expert Panel

enthalten in: Genetics in medicine : official journal of the American College of Medical Genetics | 2019

von Shen, J. | Oza, A. | Del Castillo, I. | +49

3

Asymmetric synthesis of atropisomeric pyrazole via an enantioselective reaction of azonaphthalene with pyrazolone

enthalten in: Chemical communications (Cambridge, England) | 2019

von Yuan, H. | Li, Y. | Zhao, H. | +3

4

Enamine Catalytic Annulation of Azonaphthalenes : An Access to Indole Derivatives

enthalten in: Organic letters | 2019

von Zhao, H. | Yuan, H. | Zhang, Y. | +2

5

Detecting novel mutations and combined Klinefelter syndrome in Usher syndrome cases

enthalten in: Acta oto-laryngologica | 2019

von Li, X. | Huang, S. | Yuan, Y. | +6

6

Identification of a complex genomic rearrangement in TMPRSS3 by massively parallel sequencing in Chinese cases with prelingual hearing loss

enthalten in: Molecular genetics & genomic medicine | 2019

von Li, X. | Tan, B. | Wang, X. | +11

7

Combination of Traditional Chinese Medicine and Low-Molecular-Weight Heparin Prevents Deep Vein Thrombosis After Surgery : A Meta-Analysis

enthalten in: Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis | 2019

von Chen, C. | Tang, Q. | Zhang, W. | +5

8

Identification of a complex genomic rearrangement in TMPRSS3 by massively parallel sequencing in Chinese cases with prelingual hearing loss

enthalten in: Molecular Genetics & Genomic Medicine | 2019

von Li, X. | Tan, B. | Wang, X. | +11

9

Novel OTOF gene mutations identified using a massively parallel DNA sequencing technique in DFNB9 deafness

enthalten in: Acta oto-laryngologica | 2018

von Wang, Y. | Lu, Y. | Cheng, J. | +3

10

Identification of a novel TCOF1 mutation in a Chinese family with Treacher Collins syndrome

enthalten in: Experimental and therapeutic medicine | 2018

von Yan, Z. | Lu, Y. | Wang, Y. | +5

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