Detalhe da pesquisa
1.
Synthesis of Double Trivalent Perovskite Quantum Dots Cs3BiSbX9 (X = Cl, Br, I) for Efficient CO2 Photoreduction Performance.
Small
; : e2401301, 2024 Apr 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-38671565
2.
A Low-Noble-Metal Ru@CoMn2O4 Spinel Catalyst for the Efficient Oxidation of Propane.
Molecules
; 29(10)2024 May 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-38792116
3.
[Clinical and genetic analysis of ten Chinese pedigrees affected with 7q11.23 duplication syndrome].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 41(2): 140-144, 2024 Feb 10.
Artigo
em Chinês
| MEDLINE | ID: mdl-38311550
4.
The uncertainty of copy number variants: pregnancy decisions and clinical follow-up.
Am J Obstet Gynecol
; 229(2): 170.e1-170.e8, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-36716986
5.
[Application of low-depth whole genome sequencing for copy number variation analysis in children with disorders of sex development].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 40(2): 195-201, 2023 Feb 10.
Artigo
em Chinês
| MEDLINE | ID: mdl-36709940
6.
[Clinical phenotype and genetic analysis of a patient with a heterozygous 6p25.3 deletion and partial trisomy 15q].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 40(8): 1028-1031, 2023 Aug 10.
Artigo
em Chinês
| MEDLINE | ID: mdl-37532506
7.
[Genetic analysis of a rare case with Disorder of sex development due to structural rearrangement of Y chromosome].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 40(11): 1430-1435, 2023 Nov 10.
Artigo
em Chinês
| MEDLINE | ID: mdl-37906155
8.
[Analysis of genome copy number variations in fetuses with isolated ventricular septal defect and a literature review].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 40(3): 317-321, 2023 Mar 10.
Artigo
em Chinês
| MEDLINE | ID: mdl-36854407
9.
[Genetic analysis of a pregnant woman with moderate intellectual disability due to variant of DLG4 gene].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 40(3): 354-359, 2023 Mar 10.
Artigo
em Chinês
| MEDLINE | ID: mdl-36854414
10.
Individual [18F]FDG PET and functional MRI based on simultaneous PET/MRI may predict seizure recurrence after temporal lobe epilepsy surgery.
Eur Radiol
; 32(6): 3880-3888, 2022 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-35024947
11.
[18F]FDG PET/MRI and magnetoencephalography may improve presurgical localization of temporal lobe epilepsy.
Eur Radiol
; 32(5): 3024-3034, 2022 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-34651211
12.
Combined [18F]FDG-PET with MRI structural patterns in predicting post-surgical seizure outcomes in temporal lobe epilepsy patients.
Eur Radiol
; 32(12): 8423-8431, 2022 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-35713664
13.
[Analysis of chromosomal copy number variations among 163 fetuses with echogenic bowel by using CNV-seq technology].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 39(9): 954-957, 2022 Sep 10.
Artigo
em Chinês
| MEDLINE | ID: mdl-36082564
14.
[Prenatal diagnosis and genetic counselling for a pedigree carrying a large fragment deletion of 13q].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 39(3): 334-337, 2022 Mar 10.
Artigo
em Chinês
| MEDLINE | ID: mdl-35315048
15.
[CNV-seq analysis of copy number variations in 217 fetuses with nasal bone dysplasia].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 39(10): 1076-1079, 2022 Oct 10.
Artigo
em Chinês
| MEDLINE | ID: mdl-36184086
16.
Assessment of localization accuracy and postsurgical prediction of simultaneous 18F-FDG PET/MRI in refractory epilepsy patients.
Eur Radiol
; 31(9): 6974-6982, 2021 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-33638688
17.
The potential of expanded noninvasive prenatal screening for detection of microdeletion and microduplication syndromes.
Prenat Diagn
; 41(10): 1332-1342, 2021 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-34181751
18.
[Prenatal diagnosis and family analysis of 22q11.2 microdeletion syndrome].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 38(7): 659-662, 2021 Jul 10.
Artigo
em Chinês
| MEDLINE | ID: mdl-34247372
19.
[Clinical phenotype and genetic analysis of MECP2 duplication syndrome].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 38(12): 1190-1193, 2021 Dec 10.
Artigo
em Chinês
| MEDLINE | ID: mdl-34839504
20.
[Prenatal cytogenetic and molecular genetic analysis of a fetus with confined placenta mosaicism for trisomy 16].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 38(8): 771-774, 2021 Aug 10.
Artigo
em Chinês
| MEDLINE | ID: mdl-34365622