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1.
Evaluation of the Z-score accuracy of noninvasive prenatal testing for fetal trisomies 13, 18 and 21 at a single center.
Prenat Diagn
; 41(6): 690-696, 2021 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-33480032
2.
CRISPR/Cas9 gene correction of HbH-CS thalassemia-induced pluripotent stem cells.
Ann Hematol
; 98(12): 2661-2671, 2019 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-31495903
3.
Indications for prenatal diagnosis and pregnancy outcomes of Turner syndrome with different karyotypes in 205 cases / 中华围产医学杂志
Chinese Journal of Perinatal Medicine
; (12): 41-47, 2023.
Artículo
en Zh
| WPRIM | ID: wpr-995061
4.
Parental origin of prenatally diagnosed pathogenic copy number variation in 56 pedigrees / 中华围产医学杂志
Chinese Journal of Perinatal Medicine
; (12): 360-365, 2022.
Artículo
en Zh
| WPRIM | ID: wpr-933928
5.
Prenatal diagnosis and pregnancy outcome of increased nuchal translucency with or without nuchal cystic hygroma in fetuses during first trimester / 中华围产医学杂志
Chinese Journal of Perinatal Medicine
; (12): 104-109, 2022.
Artículo
en Zh
| WPRIM | ID: wpr-933887
6.
Prenatal diagnosis and clinical outcomes of 297 fetuses with conotruncal defects / 中华妇产科杂志
Chinese Journal of Obstetrics and Gynecology
; (12): 25-31, 2022.
Artículo
en Zh
| WPRIM | ID: wpr-932421
7.
Genetic analysis and prenatal diagnosis of a fetus with Xq25 microduplication / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 425-427, 2022.
Artículo
en Zh
| WPRIM | ID: wpr-928434
8.
A qualitative research on symptom experience in patients with acute coronary syndrome before diagnosis / 中国实用护理杂志
Chinese Journal of Practical Nursing
; (36): 2261-2267, 2021.
Artículo
en Zh
| WPRIM | ID: wpr-908236
9.
Analysis of families with fetal congenital abnormalities but negative prenatal diagnosis by whole exome sequencing / 中华妇产科杂志
Chinese Journal of Obstetrics and Gynecology
; (12): 458-466, 2021.
Artículo
en Zh
| WPRIM | ID: wpr-910158
10.
Application of whole exome sequencing technology in fetuses with congenital structural abnormalities / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 900-906, 2021.
Artículo
en Zh
| WPRIM | ID: wpr-921966
11.
Consistency between quantitative fluorescent-polymerase chain reaction and karyotyping in prenatal diagnosis / 中华围产医学杂志
Chinese Journal of Perinatal Medicine
; (12): 400-404, 2020.
Artículo
en Zh
| WPRIM | ID: wpr-871078
12.
The real experience of patients with enteral nutrition after gastro/jejunostomy and their caregivers: a qualitative research Meta-synthesis / 中国实用护理杂志
Chinese Journal of Practical Nursing
; (36): 1353-1360, 2020.
Artículo
en Zh
| WPRIM | ID: wpr-864594
13.
Application of chromosomal microarray analysis in 815 fetuses with increased nuchal translucency during early pregnancy / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 833-838, 2020.
Artículo
en Zh
| WPRIM | ID: wpr-826476
14.
De Novo and Inherited SETD1A Variants in Early-onset Epilepsy / 神经科学通报·英文版
Neuroscience Bulletin
; (6): 1045-1057, 2019.
Artículo
en Inglés
| WPRIM | ID: wpr-776444
15.
Analysis of 26 fetuses with congenital anomalies of the kidney and urinary tract by whole exome sequencing / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 856-859, 2018.
Artículo
en Zh
| WPRIM | ID: wpr-775820
16.
Chorionic villus cell culture and karyotype analysis in 1983 cases of spontaneous miscarriage / 中华妇产科杂志
Chinese Journal of Obstetrics and Gynecology
; (12): 461-466, 2017.
Artículo
en Zh
| WPRIM | ID: wpr-618122
17.
Application of chromosome microarray analysis in 489 children with developmental delay/intellectual disability / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 528-533, 2017.
Artículo
en Zh
| WPRIM | ID: wpr-335090
18.
Relationship between absent or hypoplastic fetal nasal bone and chromosome abnormalities: analysis of 187 cases / 中华围产医学杂志
Chinese Journal of Perinatal Medicine
; (12): 339-342, 2015.
Artículo
en Zh
| WPRIM | ID: wpr-469119
19.
Application of whole-genome and high-resolution chromosome microarray analysis for the investigation of fetuses with ultrasound abnormalities / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 169-174, 2015.
Artículo
en Zh
| WPRIM | ID: wpr-239513
20.
The prenatal ultrasound and magnatic resonance imaging characteristics of fetal intracranial hemorrhage / 中华医学超声杂志(电子版)
Chinese Journal of Medical Ultrasound (Electronic Edition)
; (12): 383-389, 2015.
Artículo
en Zh
| WPRIM | ID: wpr-637300