Detalhe da pesquisa
1.
Association between placental DNA methylation and fetal congenital heart disease.
Mol Genet Genomics
; 298(1): 243-251, 2023 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-36396788
2.
[Analysis of MYRF gene variant in a fetus with Cardiac-urogenital syndrome].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 40(5): 563-567, 2023 May 10.
Artigo
em Zh
| MEDLINE | ID: mdl-37102290
3.
[Clinical and genetic characteristics of 12 cases of Loeys-Dietz syndrome].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 40(9): 1093-1099, 2023 Sep 10.
Artigo
em Zh
| MEDLINE | ID: mdl-37643954
4.
A novel intron mutation in FBN-1 gene identified in a pregnant woman with Marfan syndrome.
Hereditas
; 158(1): 6, 2021 Jan 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33407909
5.
Pressure-induced unexpected -2 oxidation states of bromine and superconductivity in magnesium bromide.
Phys Chem Chem Phys
; 22(5): 3066-3072, 2020 Feb 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31965119
6.
Pressure-Induced Stable Binary Compounds of Magnesium and Germanium.
Chemistry
; 24(70): 18757-18761, 2018 Dec 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-30300923
7.
The Structure and Properties of Magnesium-Phosphorus Compounds Under Pressure.
Chemistry
; 24(44): 11402-11406, 2018 Aug 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-29855104
8.
Regarding "The Role of Minimally Invasive Surgery in the Care of Women with Ovarian Cancer: A Systematic Review and Meta-analysis".
J Minim Invasive Gynecol
; 29(10): 1197, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35940523
9.
Generation of a TSC2 knockout embryonic stem cell line by CRISPR/Cas9 editing.
Stem Cell Res
; 77: 103399, 2024 Mar 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-38574666
10.
Enhancement and Broadening of the Internal Electric Field of Hole-Transport-Layer-Free Perovskite Solar Cells by Quantum Dot Interface Modification.
ACS Appl Mater Interfaces
; 16(5): 6665-6673, 2024 Feb 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-38288745
11.
Prognostic significance of IDH mutation in adult low-grade gliomas: a meta-analysis.
J Neurooncol
; 113(2): 277-84, 2013 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-23504258
12.
Genetic aetiology distribution of 398 foetuses with congenital heart disease in the prenatal setting.
ESC Heart Fail
; 10(2): 917-930, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36478645
13.
Expanding the phenotype associated with SMARCC2 variants: a fetus with tetralogy of Fallot.
BMC Med Genomics
; 15(1): 40, 2022 03 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-35241061
14.
Diverse cardiac phenotypes among different carriers of the same MYH7 splicing variant allele (c.732+1G>A) from a family.
BMC Med Genomics
; 15(1): 36, 2022 02 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-35209905
15.
Case Report: Biventricular Noncompaction Cardiomyopathy With Pulmonary Stenosis and Bradycardia in a Fetus With KCNH2 Mutation.
Front Genet
; 13: 821226, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35281812
16.
Placental DNA Methylation Abnormalities in Prenatal Conotruncal Heart Defects.
Front Genet
; 13: 878063, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35646082
17.
Genetic abnormalities in fetal congenital heart disease with aberrant right subclavian artery.
Sci Rep
; 12(1): 15899, 2022 09 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-36151134
18.
Genetic and Clinical Features of Heterotaxy in a Prenatal Cohort.
Front Genet
; 13: 818241, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35518361
19.
Detection of TSC1/TSC2 mosaic variants in patients with cardiac rhabdomyoma and tuberous sclerosis complex by hybrid-capture next-generation sequencing.
Mol Genet Genomic Med
; 9(10): e1802, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34480426
20.
Unique dual indexing PCR reduces chimeric contamination and improves mutation detection in cell-free DNA of pregnant women.
Talanta
; 217: 121035, 2020 Sep 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32498851