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Clinical Genetics
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March 4, 2008
Novel mutations in the vWFA2 domain of COCH in two Chinese DFNA9 families
H J Yuan, D Y Han, Q Sun, et al.
Clinical Genetics
|
September 18, 2007
A novel DFNA5 mutation, IVS8+4 A>G, in the splice donor site of intron 8 causes late-onset non-syndromic hearing loss in a Chinese family
J Cheng, D Y Han, P Dai, et al.
Nature Genetics
|
December 8, 1998
Mutations in the gene encoding gap junction protein beta-3 associated with autosomal dominant hearing impairment
J H Xia, C Y Liu, B S Tang, et al.
Zhonghua Yi Xue Za Zhi
|
July 30, 2024
[Interim efficacy of a multicenter cohort study for China Net Childhood Lymphoma mature B-cell lymphoma 2017 regimen in the treatment of pediatric High-grade-B cell lymphoma]
Y Zhao, S Huang, Y P Jia, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics
|
September 27, 2024
[A multicenter study on effect of delayed chemotherapy on prognosis of Burkitt lymphoma in children]
L Song, L Jin, Y H Zhang, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics
|
October 8, 2022
[Mid-term efficacy of China Net Childhood Lymphoma-mature B-cell lymphoma 2017 regimen in the treatment of pediatric Burkitt lymphoma]
M Zhang, P Wu, Y L Duan, et al.
Physical Review Letters
|
May 21, 2010
Measurements of h(c)(1P(1)) in psi' decays
M Ablikim, M N Achasov, L An, et al.
Physical Review Letters
|
January 15, 2011
Evidence for ψ' decays into γπ0 and γη
M Ablikim, M N Achasov, L An, et al.
Physical Review Letters
|
March 17, 2011
Confirmation of the X(1835) and observation of the resonances X(2120) and X(2370) in J/ψ→γπ+π-η'
M Ablikim, M N Achasov, L An, et al.
Physical Review Letters
|
September 21, 2011
Observation of χ(c1) decays into vector meson pairs φφ, ωω, and ωφ
M Ablikim, M N Achasov, L An, et al.
Page
of 37
Search research articles
Search
Showing results (221-230 of 365) with videos related to
Sort By:
Page
of 37
Clinical Genetics
|
March 4, 2008
Novel mutations in the vWFA2 domain of COCH in two Chinese DFNA9 families
H J Yuan, D Y Han, Q Sun, et al.
Clinical Genetics
|
September 18, 2007
A novel DFNA5 mutation, IVS8+4 A>G, in the splice donor site of intron 8 causes late-onset non-syndromic hearing loss in a Chinese family
J Cheng, D Y Han, P Dai, et al.
Nature Genetics
|
December 8, 1998
Mutations in the gene encoding gap junction protein beta-3 associated with autosomal dominant hearing impairment
J H Xia, C Y Liu, B S Tang, et al.
Zhonghua Yi Xue Za Zhi
|
July 30, 2024
[Interim efficacy of a multicenter cohort study for China Net Childhood Lymphoma mature B-cell lymphoma 2017 regimen in the treatment of pediatric High-grade-B cell lymphoma]
Y Zhao, S Huang, Y P Jia, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics
|
September 27, 2024
[A multicenter study on effect of delayed chemotherapy on prognosis of Burkitt lymphoma in children]
L Song, L Jin, Y H Zhang, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics
|
October 8, 2022
[Mid-term efficacy of China Net Childhood Lymphoma-mature B-cell lymphoma 2017 regimen in the treatment of pediatric Burkitt lymphoma]
M Zhang, P Wu, Y L Duan, et al.
Physical Review Letters
|
May 21, 2010
Measurements of h(c)(1P(1)) in psi' decays
M Ablikim, M N Achasov, L An, et al.
Physical Review Letters
|
January 15, 2011
Evidence for ψ' decays into γπ0 and γη
M Ablikim, M N Achasov, L An, et al.
Physical Review Letters
|
March 17, 2011
Confirmation of the X(1835) and observation of the resonances X(2120) and X(2370) in J/ψ→γπ+π-η'
M Ablikim, M N Achasov, L An, et al.
Physical Review Letters
|
September 21, 2011
Observation of χ(c1) decays into vector meson pairs φφ, ωω, and ωφ
M Ablikim, M N Achasov, L An, et al.
Page
of 37