Search details
1.
A case of self-improving collodion ichthyosis in Vietnam.
Pediatr Dermatol
; 37(3): 574-575, 2020 May.
Article
in English
| MEDLINE | ID: mdl-32105361
2.
Acromesomelic dysplasia Maroteaux-type in patients from Vietnam.
Am J Med Genet A
; 179(8): 1420-1422, 2019 08.
Article
in English
| MEDLINE | ID: mdl-31077548
3.
Diagnosis and Management of a Patient With Primary Hypertrophic Osteoarthropathy With SCLO2A1 Pathogenic Variants in Vietnam.
J Clin Rheumatol
; 27(8S): S739-S740, 2021 Dec 01.
Article
in English
| MEDLINE | ID: mdl-32833909
4.
Mutation characteristic of 103 haemophilia A patients in Vietnam: Identification of novel mutations.
Haemophilia
; 25(4): e274-e277, 2019 Jul.
Article
in English
| MEDLINE | ID: mdl-30913330
5.
Application of short tandem repeats (STRs) in the preimplantation genetic diagnosis (PGD) of α-thalassemia.
Taiwan J Obstet Gynecol
; 63(3): 375-380, 2024 May.
Article
in English
| MEDLINE | ID: mdl-38802201
6.
A novel IGHMBP2 variant and clinical diversity in Vietnamese SMARD1 and CMT2S patients.
Front Pediatr
; 12: 1165492, 2024.
Article
in English
| MEDLINE | ID: mdl-38415210
7.
Targeted next-generation sequencing determined a novel SGCG variant that is associated with limb-girdle muscular dystrophy type 2C: A case report.
Clin Case Rep
; 11(3): e7025, 2023 Mar.
Article
in English
| MEDLINE | ID: mdl-36992678
8.
In silico validation revealed the role of SCN5A mutations and their genotype-phenotype correlations in Brugada syndrome.
Mol Genet Genomic Med
; 11(12): e2263, 2023 Dec.
Article
in English
| MEDLINE | ID: mdl-37547970
9.
Mutation spectrum of retinoblastoma patients in Vietnam.
Mol Genet Genomic Med
; 11(11): e2244, 2023 Nov.
Article
in English
| MEDLINE | ID: mdl-37548407
10.
Establishing a national program for fetoscopic guided laser occlusion for twin-to-twin transfusion syndrome in Sweden.
Acta Obstet Gynecol Scand
; 91(10): 1196-200, 2012 Oct.
Article
in English
| MEDLINE | ID: mdl-22568938
11.
Information related to prenatal genetic counseling: interpretation by adolescents, effects on risk perception and ethical implications.
J Genet Couns
; 21(4): 536-46, 2012 Aug.
Article
in English
| MEDLINE | ID: mdl-22037899
12.
Prenatal diagnosis of atrioventricular discordance with ventriculoarterial concordance by fetal echocardiography: A case report.
Taiwan J Obstet Gynecol
; 61(2): 372-377, 2022 Mar.
Article
in English
| MEDLINE | ID: mdl-35361405
13.
Whole exome sequencing analysis in a couple with three children who died prematurely due to carnitine-acylcarnitine translocase deficiency.
Taiwan J Obstet Gynecol
; 61(1): 153-156, 2022 Jan.
Article
in English
| MEDLINE | ID: mdl-35181030
14.
Feasibility of combining short tandem repeats (STRs) haplotyping with preimplantation genetic diagnosis (PGD) in screening for beta thalassemia.
PLoS One
; 17(12): e0278539, 2022.
Article
in English
| MEDLINE | ID: mdl-36476827
15.
Molecular Characterization and Genotype-Phenotype Correlation of G6PD Mutations in Five Ethnicities of Northern Vietnam.
Anemia
; 2022: 2653089, 2022.
Article
in English
| MEDLINE | ID: mdl-35845714
16.
Preimplantation genetic testing (PGT) for hemophilia A: Experience from one center.
Taiwan J Obstet Gynecol
; 61(6): 1009-1014, 2022 Nov.
Article
in English
| MEDLINE | ID: mdl-36427965
17.
More appreciation of life or regretting the test? Experiences of living as a mutation carrier of Huntington's disease.
J Genet Couns
; 20(1): 70-9, 2011 Feb.
Article
in English
| MEDLINE | ID: mdl-20878217
18.
Procedure-related complications and perinatal outcome after intrauterine transfusions in red cell alloimmunization in Stockholm.
Fetal Diagn Ther
; 30(4): 266-73, 2011.
Article
in English
| MEDLINE | ID: mdl-22024691
19.
Microcephaly primary hereditary (MCPH): Report of novel ASPM variants and prenatal diagnosis in a Vietnamese family.
Taiwan J Obstet Gynecol
; 60(5): 907-910, 2021 Sep.
Article
in English
| MEDLINE | ID: mdl-34507672
20.
Characterization of double ring chromosome 4 mosaicism associated with bilateral hip dislocation, cortical dysgenesis, and epilepsy.
Am J Med Genet A
; 149A(12): 2782-7, 2009 Dec.
Article
in English
| MEDLINE | ID: mdl-19921639