Detalhe da pesquisa
1.
MBD5-related intellectual disability in a Vietnamese child.
Am J Med Genet A;
185(4): 1321-1323, 2021 04.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33427406
2.
Y chromosome damage underlies testicular abnormalities in ATR-X syndrome.
iScience;
27(5): 109629, 2024 May 17.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38616920
3.
MFSD7c functions as a transporter of choline at the blood-brain barrier.
Cell Res;
34(3): 245-257, 2024 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38302740
4.
An extremely rare missense mutation of the androgen receptor gene in a Vietnamese family with complete androgen insensitivity syndrome.
Nagoya J Med Sci;
85(2): 362-368, 2023 May.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37346838
5.
An Extremely Rare SRD5A2 Gene c.485A>C Mutation in a Compound Heterozygous Newborn with Disorders of Sex Development First Identified in Vietnam.
Case Rep Endocrinol;
2022: 6025916, 2022.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35386187
6.
Mfsd2b and Spns2 are essential for maintenance of blood vessels during development and in anaphylactic shock.
Cell Rep;
40(7): 111208, 2022 08 16.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35977478
7.
An experience in prenatal diagnosis via QF-PCR of a female child with a 9.9 Mb pure deletion at 18p11.32-11.22.
Nagoya J Med Sci;
82(4): 783-790, 2020 Nov.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33311808
8.
Association of TP53 gene codon 72 polymorphism with Helicobacter pylori-positive non-cardia gastric cancer in Vietnam.
J Infect Dev Ctries;
13(11): 984-991, 2019 11 30.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32087070