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1.
Strong enhancement of Goos-Hänchen shift through the resonant optical tunneling effect.
Opt Express
; 30(26): 47338-47349, 2022 Dec 19.
Artículo
en Inglés
| MEDLINE | ID: mdl-36558664
2.
Communication wavelength investigation of bound states in the continuum of one-dimensional two-material periodic ring optical waveguide network.
Opt Express
; 30(21): 37888-37898, 2022 Oct 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-36258368
3.
Chromosomal abnormality: Prevalence, prenatal diagnosis and associated anomalies based on a provincial-wide birth defects monitoring system.
J Obstet Gynaecol Res
; 47(3): 865-872, 2021 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-33372274
4.
The pomegranate (Punica granatum L.) draft genome dissects genetic divergence between soft- and hard-seeded cultivars.
Plant Biotechnol J
; 18(4): 955-968, 2020 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-31549477
5.
Prenatal diagnosis of birth defects and termination of pregnancy in Hunan Province, China.
Prenat Diagn
; 40(8): 925-930, 2020 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-31955435
6.
Identification of the SUT Gene Family in Pomegranate (Punica granatum L.) and Functional Analysis of PgL0145810.1.
Int J Mol Sci
; 21(18)2020 Sep 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-32927615
7.
Small RNA and mRNA Sequencing Reveal the Roles of microRNAs Involved in Pomegranate Female Sterility.
Int J Mol Sci
; 21(2)2020 Jan 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-31952315
8.
Three novel mutations of STK11 gene in Chinese patients with Peutz-Jeghers syndrome.
BMC Med Genet
; 17(1): 77, 2016 Nov 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-27821076
9.
De novo exonic deletion of KDM6A in a Chinese girl with Kabuki syndrome: A case report and brief literature review.
Am J Med Genet A
; 170(6): 1613-21, 2016 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-27028180
10.
[Analysis of CGG repeat instability in germline cells from two male fetuses affected with fragile X syndrome].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 33(5): 606-9, 2016 Oct.
Artículo
en Zh
| MEDLINE | ID: mdl-27577204
11.
Noninvasive prenatal testing for Wilson disease by use of circulating single-molecule amplification and resequencing technology (cSMART).
Clin Chem
; 61(1): 172-81, 2015 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-25376582
12.
The first case of a non-infertile female patient with Pitt-Hopkins syndrome.
Am J Med Genet A
; 179(11): 2311-2314, 2019 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-31464085
13.
[Phenotype-genotype correlation analysis of 12 cases with Angelman/Prader-Willi syndrome].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 31(6): 708-12, 2014 Dec.
Artículo
en Zh
| MEDLINE | ID: mdl-25449072
14.
Global and regional trends in the incidence and mortality burden of endometrial cancer, 1990-2019: Updated results from the Global Burden of Disease Study, 2019.
Chin Med J (Engl)
; 137(3): 294-302, 2024 Feb 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-37874032
15.
Evaluating ClinGen variant curation expert panels' application of PVS1 code.
Eur J Med Genet
; 67: 104909, 2024 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-38199457
16.
Non-invasive prenatal testing of fetal whole chromosome aneuploidy by massively parallel sequencing.
Prenat Diagn
; 33(5): 409-15, 2013 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-23299662
17.
Trends in incidence and mortality for ovarian cancer in China from 1990 to 2019 and its forecasted levels in 30 years.
J Ovarian Res
; 16(1): 139, 2023 Jul 14.
Artículo
en Inglés
| MEDLINE | ID: mdl-37452315
18.
The comprehensive analysis of thalassemia alleles (CATSA) based on single-molecule real-time technology (SMRT) is a more powerful strategy in the diagnosis of thalassemia caused by rare variants.
Clin Chim Acta
; 551: 117619, 2023 Nov 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-38375625
19.
Disrupting reconsolidation by PKA inhibitor in BLA reduces heroin-seeking behavior.
Front Cell Neurosci
; 16: 996379, 2022.
Artículo
en Inglés
| MEDLINE | ID: mdl-36106011
20.
The Role of Microtubule Associated Serine/Threonine Kinase 3 Variants in Neurodevelopmental Diseases: Genotype-Phenotype Association.
Front Mol Neurosci
; 14: 775479, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-35095415