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1.
TMEM151A Variants Cause Paroxysmal Kinesigenic Dyskinesia: A Large-Sample Study.
Mov Disord
; 37(3): 545-552, 2022 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-34820915
2.
Large-area flexible MWCNT/PDMS pressure sensor for ergonomic design with aid of deep learning learning.
Nanotechnology
; 33(34)2022 May 31.
Artículo
en Inglés
| MEDLINE | ID: mdl-35417891
3.
[A consensus on the standardization of the next generation sequencing process for the diagnosis of genetic diseases (1) - Procedures prior to genetic testing].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 37(3): 334-338, 2020 Mar 10.
Artículo
en Zh
| MEDLINE | ID: mdl-32128754
4.
[A consensus on the standardization of the next generation sequencing process for the diagnosis of genetic diseases (3) - Data analysis].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 37(3): 345-351, 2020 Mar 10.
Artículo
en Zh
| MEDLINE | ID: mdl-32128756
5.
[A consensus on the standardization of the next generation sequencing process for the diagnosis of genetic diseases (4) - Report interpretation and genetic counseling].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 37(3): 352-357, 2020 Mar 10.
Artículo
en Zh
| MEDLINE | ID: mdl-32128757
6.
[An overview of tools for post-analysis of high-throughput sequencing data in clinical study].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 36(5): 508-512, 2019 May 10.
Artículo
en Zh
| MEDLINE | ID: mdl-31030446
7.
[Discussion on the standard of clinical genetic testing report and the consensus of gene testing industry].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 35(1): 1-8, 2018 Feb 10.
Artículo
en Zh
| MEDLINE | ID: mdl-29419850
8.
Alteration of gene expression profiling including GPR174 and GNG2 is associated with vasovagal syncope.
Pediatr Cardiol
; 36(3): 475-80, 2015 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-25367286
9.
mvPPT: A Highly Efficient and Sensitive Pathogenicity Prediction Tool for Missense Variants.
Genomics Proteomics Bioinformatics
; 21(2): 414-426, 2023 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-35940520
10.
A Novel Heterozygous Missense Variant in Parathyroid Hormone 1 is Related to the Occurrence of Developmental Dysplasia of the Hip.
Genet Test Mol Biomarkers
; 27(3): 74-80, 2023 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-36989525
11.
Establishment of an improved high-efficiency thermal asymmetric interlaced PCR for identification of genomic integration sites mediated by phiC31 integrase.
World J Microbiol Biotechnol
; 28(3): 1295-9, 2012 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-22805850
12.
Textile-Based Mechanical Sensors: A Review.
Materials (Basel)
; 14(20)2021 Oct 14.
Artículo
en Inglés
| MEDLINE | ID: mdl-34683661
13.
A multiplex ligationdependent probe amplificationbased nextgeneration sequencing approach for the detection of copy number variations in the human genome.
Mol Med Rep
; 18(6): 5823-5833, 2018 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-30365071
14.
A recurrent mutation in bone morphogenetic proteins-2-inducible kinase gene is associated with developmental dysplasia of the hip.
Exp Ther Med
; 13(5): 1773-1778, 2017 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-28565766
15.
A gain-of-function ACTC1 3'UTR mutation that introduces a miR-139-5p target site may be associated with a dominant familial atrial septal defect.
Sci Rep
; 6: 25404, 2016 05 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-27139165
16.
A profile of native integration sites used by φC31 integrase in the bovine genome.
J Genet Genomics
; 39(5): 217-24, 2012 May 20.
Artículo
en Inglés
| MEDLINE | ID: mdl-22624883
17.
Application of high-resolution melting for genotyping bovine mitochondrial DNA.
Biotechnol Prog
; 27(2): 592-5, 2011.
Artículo
en Inglés
| MEDLINE | ID: mdl-21448913
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