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科研机构
山东大学 [3]
北京大学 [2]
华南理工大学 [1]
内容类型
期刊论文 [5]
会议论文 [1]
发表日期
2015 [6]
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Live births after simultaneous avoidance of monogenic diseases and chromosome abnormality by next-generation sequencing with linkage analyses
期刊论文
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2015
Yan, Liying
;
Huang, Lei
;
Xu, Liya
;
Huang, Jin
;
Ma, Fei
;
Zhu, Xiaohui
;
Tang, Yaqiong
;
Liu, Mingshan
;
Lian, Ying
;
Liu, Ping
;
Li, Rong
;
Lu, Sijia
;
Tang, Fuchou
;
Qiao, Jie
;
Xie, X. Sunney
收藏
  |  
浏览/下载:7/0
  |  
提交时间:2017/12/03
monogenic diseases
chromosome abnormality
IVF
PGD
MALBAC
PREIMPLANTATION GENETIC DIAGNOSIS
GENOME AMPLIFICATION
HUMAN BLASTOCYSTS
REAL-TIME
IN-VITRO
ANEUPLOIDY
EMBRYOS
PGD
DISORDERS
CELLS
Single-Cell Whole-Genome Amplification and Sequencing: Methodology and Applications
期刊论文
ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS, VOL 16, 2015
Huang, Lei
;
Ma, Fei
;
Chapman, Alec
;
Lu, Sijia
;
Xie, Xiaoliang Sunney
收藏
  |  
浏览/下载:2/0
  |  
提交时间:2017/12/03
single-cell genomics
cancer genomics
WGA
DOP-PCR
MDA
MALBAC
CTC
PGD
PGS
in vitro fertilization
PREIMPLANTATION GENETIC DIAGNOSIS
CIRCULATING TUMOR-CELLS
COPY-NUMBER
DNA-POLYMERASE
HYPERTROPHIC CARDIOMYOPATHY
HUMAN RECOMBINATION
HAPLOTYPE MAP
SPERM CELLS
CANCER
ANEUPLOIDY
Clinical Considerations of Preimplantation Genetic Diagnosis for Monogenic Diseases
期刊论文
PLOS ONE, 2015, 卷号: 10
作者:
Hu, Xiaokun
;
Wang, Jing
;
Li, Yubin
;
Wang, Yizi
;
Ding, Chenhui
收藏
  |  
浏览/下载:6/0
  |  
提交时间:2019/04/25
Reproductive management through integration of PGD and MPS-based noninvasive prenatal screening/diagnosis for a family with GJB2-associated hearing impairment
期刊论文
中国科学. 生命科学, 2015, 卷号: 58, 期号: 9, 页码: 829-838
作者:
Xiong WenPing
;
Wang DaYong
;
Gao Yuan
;
Gao Ya
;
Wang HongYang
收藏
  |  
浏览/下载:13/0
  |  
提交时间:2019/12/17
preimplantation genetic diagnosis (PGD)
noninvasive prenatal testing
(NIPT)
noninvasive prenatal diagnosis (NIPD)
GJB2 (encoding the gap
junction protein connexin 26)
hearing impairment
Reproductive management through integration of PGD and MPS-based noninvasive prenatal screening/diagnosis for a family with GJB2-associated hearing impairment
期刊论文
Science China(Life Sciences), 2015, 期号: 09, 页码: 829-842
作者:
XIONG WenPing
;
WANG DaYong
;
GAO Yuan
;
GAO Ya
;
WANG HongYang
收藏
  |  
浏览/下载:9/0
  |  
提交时间:2019/12/17
preimplantation genetic diagnosis(PGD)
noninvasive prenatal testing(NIPT)
noninvasive prenatal diagnosis(NIPD)
GJB2(encoding the
First healthy baby born after PGD (preimplantation genetic diagnosis) - noninvasive haplotype screening in couples both carrying deafness gene GJB2 mutation
会议论文
31st Annual Meeting of the European-Society-of-Human-Reproduction-and-Embryology (ESHRE), JUN 14-17, 2015
作者:
Chen, Z.
;
Gao, Y.
;
Huang, S.
;
Yan, J.
;
Li, J.
收藏
  |  
浏览/下载:11/0
  |  
提交时间:2019/12/31
congenital hearing loss
preimplantation genetic diagnosis
haplotyping
screening
GJB2 Gene
aneuploidy screening
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